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It is evident that site-specific systemic drug delivery can reduce side effects, systemic toxicity, and minimal dosage requirements predominantly by delivering drugs to particular pathological sites, cells, and even subcellular structures. The endoplasmic reticulum (ER) and associated cell organelles play a vital role in several essential cellular functions and activities, such as the synthesis of lipids, steroids, membrane-associated proteins along with intracellular transport, signaling of Ca2+, and specific response to stress. Therefore, the dysfunction of ER is correlated with numerous diseases where cancer, neurodegenerative disorders, diabetes mellitus, hepatic disorder, etc., are very common. To achieve satisfactory therapeutic results in certain diseases, it is essential to engineer delivery systems that can effectively enter the cells and target ER. Nanoparticles are highly biocompatible, contain a variety of cargos or payloads, and can be modified in a pliable manner to achieve therapeutic effectiveness at the subcellular level when delivered to specific organelles. Passive targeting drug delivery vehicles, or active targeting drug delivery systems, reduce the nonselective accumulation of drugs while reducing side effects by modifying them with small molecular compounds, antibodies, polypeptides, or isolated bio-membranes. The targeting of ER and closely associated organelles in cells using nanoparticles, however, is still unsymmetrically understood. Therefore, here we summarized the pathophysiological prospect of ER stress, involvement of ER and mitochondrial response, disease related to ER dysfunctions, essential therapeutics, and nanoenabled modulation of their delivery to optimize therapy. [ABSTRACT FROM AUTHOR]

Nanotechnology offers several opportunities to improve conventional drugs to avoid issues that pharmaceutical industries are facing nowadays. Hydrophobic and hydrophilic drugs have been found to be more readily soluble in mixed polymer nanohydrogels, which improves their solubility in solution. An attempt has been made in the present study to enhance the efficacy of beta-lactam antibiotics by making nanoformulation using mixed polymer nanohydrogels derived from natural polymers sodium alginate and chitosan. As a consequence, this formulation permitted amoxicillin (MOX) to be entrapped in alginate hydrogels and, in addition, chitosan-induced cationic charges on the surface of nanoparticles. Physicochemical characterizations and swelling properties, encapsulation efficiency, MOX release profile at different pH, and MTT assay to establish the toxicity of synthesized nanocomposite were investigated. There was a significant improvement in the effectiveness of the encapsulated drug amoxicillin against Gram-negative bacteria Escherichia coli compared to the aqueous solution of the drug. It has been calculated that the encapsulation efficiency was approximately 64% by spectrophotometry, and antibiotic sensitivity tests in the presence of Gram-negative bacteria have shown that the encapsulated drug within nanohydrogels has superior antibacterial efficacy against them. This formulation with cationic surface charge may be a superior alternative to inactivate beta-lactam antibiotic-resistant Gram-negative bacteria than the standard medications available. [ABSTRACT FROM AUTHOR]

Lung cancer is managed using conventional therapies, including chemotherapy, radiation therapy, or a combination of both. Each of these therapies has its own limitations, such as the indiscriminate killing of normal as well as cancer cells, the solubility of the chemotherapeutic drugs, rapid clearance of the drugs from circulation before reaching the tumor site, the resistance of cancer cells to radiation, and over-sensitization of normal cells to radiation. Other treatment modalities include gene therapy, immunological checkpoint inhibitors, drug repurposing, and in situ cryo-immune engineering (ICIE) strategy. Nanotechnology has come to the rescue to overcome many shortfalls of conventional therapies. Some of the nano-formulated chemotherapeutic drugs, as well as nanoparticles and nanostructures with surface modifications, have been used for effective cancer cell killing and radio sensitization, respectively. Nano-enabled drug delivery systems act as cargo to deliver the sensitizer molecules specifically to the tumor cells, thereby enabling the radiation therapy to be more effective. In this review, we have discussed the different conventional chemotherapies and radiation therapies used for inhibiting lung cancer. We have also discussed the improvement in chemotherapy and radiation sensitization using nanoparticles. [ABSTRACT FROM AUTHOR]

Carbon-decorated ferrite nanodots (MNF@Cs) have been enhanced with superparamagnetism and higher fluorescence quantum yield by encapsulation with an alginate derivative to create a cost-effective and less toxic multimodal contrast agent for replacing the conventional heavy metal Gd-containing contrast agent used in MR imaging. The novel surface-engineered particles (MNF@C-OSAs), devoid of labels, can simultaneously provide both longitudinal and transverse relaxation-based magnetic resonance imaging (MRI) and fluorescence emission. According to the findings of in vitro studies, the calculated molar relaxivities and the molar radiant efficiencies are indicative of the multimodal efficacy of MNF@C-OSA as compared with MNF@C particles and conventional contrast agents used in medical imaging. MNF@C-OSAs were shown to be significantly biocompatible and negligibly toxic when assessed against A549 cells and zebrafish embryos, indicating their potential for use as theranostic agents. [ABSTRACT FROM AUTHOR]

The domain of Janus nanoparticles (JNPs) has seen a surge in research and development during the last decade. JNPs are anisotropic composite innovations with remarkable characteristics that depict a peculiar class of particles, which integrate the features and functions of multiple materials into a single unit. Janus particles are superior prospects for several high-end applications due to their possible modifications by "click chemistry". JNPs offer new possibilities by combining the features of components. Janus nanoparticles can pack multiple pharmaceuticals and imaging contrast agents simultaneously since they have a distinct chemical configuration on different sides. As a result, they become ideal for administration and bioimaging at once. They have sparked interest due to their exceptional architecture and their potential implications in science and engineering, biological application, and most notably, theranostics. The emphasis of this review is on the latest advancement in the fabrication and implementation of innovative Janus nanoparticles, along with their spectacular performance in therapeutic delivery applications. [ABSTRACT FROM AUTHOR]

Psychiatry involves the study of behavior, mind, personality, emotions, and human thoughts, which helps in the assessment and treatment of various mental health issues. Recently, the complexity of psychiatry has increased among all other medical specialties. Major depression is considered to become the global cause of disability by 2030. Antidepressants are the primary care or treatment given to any patient. Generally, antidepressants work by balancing the neurotransmitters in the brain, which accounts for the change in mood and emotions. The major problem limiting the use and research of antidepressants is blood brain barrier (BBB). They are highly selective for the movement of ions and molecules between blood and the brain. In particular circumstances, BBB hinders the entry of these drugs to the brain, thereby decreasing the efficacy, in turn increasing the side effects. Drug molecules larger than the pore size of BBB cannot pass through them. Nanopsychiatry deals with the application of nanoparticles in designing drugs, treatments, and diagnostic tools for several neurological and psychiatric illnesses. Nanoparticles exhibit a large surface-to-volume ratio which empowers them to remain a primary part of an effective drug delivery system. Nanocarriers made up of biodegradable polymers can overcome the limitations of BBB. Other than polymers, novel surfactantbased nanocarriers are a successful carrier of the drug across the BBB. This review discusses the severity of depression and the need for novel nanoassisted drug delivery systems. [ABSTRACT FROM AUTHOR]

The importance of stem cell growth and its fate is highly essential for the use of stem cells in therapy and regeneration. There are conflicting evidences regarding the actual role of stem cells when injected into a patient towards damage recovery and its lifespan inside the body. Tumor microenvironment differs from that of normal cells and may have a role in the growth of stem cells when associated with them. In cancer, the uncontrolled growth of cells remodels the extracellular matrix (ECM). The ECM alteration occurs as the mutated fibroblast cells release growth factors into the ECM which further alters the ECM directly or changes the epithelial cells and then alters the ECM. In this review we will discuss about the components and functions of ECM and how does it differ in cancer cells compared to normal cells. Abnormal dynamics of the ECM and its role in cancer progression will also be discussed. [ABSTRACT FROM AUTHOR]

Propagation of stem cells in abundance is essential for use as cell therapy in regenerative medicine. Proliferation and differentiation of stem cells are influenced by interaction between cells and their microenvironment. Extracelluar matrix (ECM) forms the chunk of niche with its components, which is remodelled by the cellular activity. The remodelling and change of ECM components have an impact on cellular activity. ECM plays a vital role in the uncontrolled proliferation of cancer cells. In the present study, we have examined the proliferative ability of mouse embryonic stem cells (C3H10 T1/2 clone 8) grown on cell-free ECM isolated from KB and MCF-7 cancer cell line cultures, separately, using standard ammonium hydroxide method. The texture of ECM was characterized from images captured with inverted microscope and scanning electron microscope (SEM). The growth of C3H10 T1/2 clone 8 cells over KB-ECM and MCF-ECM was monitored up to 192 h and the doubling time was estimated. KB-ECM promoted growth rate by reducing the doubling time from 23 to 14 h, whereas MCF-ECM prolonged the lifetime of stem cells by extending the log phase of growth. The surface topography of KBECM under SEM showed rough, irregular and meshlike structure compared to MCF-7-derived ECM. This may account for enhanced growth rate of stem cells. The findings underscore the relevance of modifications to scale-up the generation of stem cells for use in regenerative medicine. Further studies are required with different sources of stem cells grown on modified components of ECM to identify the appropriate ECM. [ABSTRACT FROM AUTHOR]

Leukemia is a cancer of blood cells that mainly affects the white blood cells. In acute myeloid leukemia (AML) sudden growth of cancerous cells occurs in blood and bone marrow, and it disrupts normal blood cell production. Most patients are asymptomatic, but it spreads rapidly and can become fatal if left untreated. AML is the prevalent form of leukemia in children. Risk factors of AML include chemical exposure, radiation, genetics, etc. Conventional diagnostic methods of AML are complete blood count tests and bone marrow aspiration, while conventional treatment methods involve chemotherapy, radiation therapy, and bone marrow transplant. There is a risk of cancer cells spreading progressively to the other organs if left untreated, and hence, early diagnosis is required. The conventional diagnostic methods are time- consuming and have drawbacks like harmful side effects and recurrence of the disease. To overcome these difficulties, nanoparticles are employed in treating and diagnosing AML. These nanoparticles can be surface- modified and can be used against cancer cells. Due to their enhanced permeability effect and high surface-to-volume ratio they will be able to reach the tumour site which cannot be reached by traditional drugs. This review article talks about how nanotechnology is more advantageous over the traditional methods in the treatment and diagnosis of AML. [ABSTRACT FROM AUTHOR]

A biosensor can sense biological elements after interaction with the recognition element. The signal produced due to interaction of the analyte with its biochemical element is transduced by a transducer and detected by appropriate modes. The miniaturization of these biosensors at the nano level using nanostructures as a platform for sensing the analyte or its detection is called a nanobiosensor. Several biological elements can be detected like nucleic acids, enzymes, antibodies, microorganisms, toxins, cells etc. with high specificity. This mini review focuses on the different types of nanobiosensors based on the type of analyte and the type of transducer used for detection. The different types of fluorescence based design of biosensors are also discussed along with the metal enhanced fluorescence based nanobiosensors. The application of biosensors towards the diagnosis of various diseases, targeted drug delivery and imaging is also discussed. [ABSTRACT FROM AUTHOR]

Zinc oxide (ZnO) is explicitly used in sunscreens and cosmetic products; however, its effect in vivo is toxic in some cases. The UV blocking efficacy of ZnO nanoparticles is lost due to photocatalysis. To isolate a lower toxic species of sunblockers, ZnO nanoparticles were synthesized and coated with chitosan – a natural polymer (ZnO–CTS) and polyethylene glycol (PEG) – a synthetic polymer (ZnO–PEG). Coating with CTS and PEG circumvented the photocatalytic activity, increased the stability and improved the UV absorption efficacy. The effect of ZnO, ZnO–CTS and ZnO–PEG nanoparticles in vivo on zebrafish embryo revealed lower deposition of ZnO–CTS and ZnO–PEG nanoparticles atop the eggs compared to ZnO. The survival of zebrafish embryos was always found to be higher in case of ZnO–CTS with respect to ZnO-treated ones. PEG coating exhibited better UV attenuation, but, in vivo it induced delayed hatching. Thus, one of the reasons for better survival could be attributed to lower aggregation of ZnO–CTS nanoparticles atop eggs thereby facilitating the breathing of embryos. [ABSTRACT FROM AUTHOR]

Abstract: Amyloid-β (Aβ) is the major constituent of senile plaques in the brains of Alzheimer''s disease patients. In order to develop an efficient in vitro system for studying the interaction of cells with Aβ aggregates, we have prepared a synthetic amyloid lawn by immobilizing Aβ peptides over a functionalized glass surface and subsequently incubating the template in a fresh Aβ solution. On the top of different types of amyloid lawns (e.g. monomeric, oligomeric, and fibrillar), we cultivated PC12 cells, creating physical contacts between the cells and the lawns. Results indicated that cell viability was differentially affected when grown atop different Aβ lawns while cells were well adhered onto the surface of these Aβ lawns. The mode of cell death by Aβ lawn was confirmed to be apoptotic rather than necrotic, showing that cells undergo suicide by just contact with Aβ lawn. While conventional ‘solution-based’ methods for testing amyloid toxicity suffer from problems such as lot-to-lot variations, continued fibrillation, and heterogeneous population of aggregates, our ‘surface-based’ lawn system is suitable for high-throughput analysis of amyloid toxicity, which may enable high-throughput screening of potential drug candidates for treating amyloid diseases with the goal of reducing the cell death on the lawn. [Copyright &y& Elsevier]

Recently discovered evidences suggest that precipitation of Alzheimer's β-amyloid (Aβ) peptide and the toxicity in Alzheimer's disease (AD) are caused by abnormal interactions with neocortical metal ions, especially Zn2+, Cu2+, and Fe3+. While many studies had focused on the role of a "single" metal ion and its interaction with Aβ peptides, such studies involving "multiple" metal ions have hardly been explored. Here, to explore the nature of codeposition of different metals, two or more metal ions along with Aβ were incubated over a solid template prepared by immobilizing Aβ42 oligomers. The influence of Zn2+, Cu2+, and Fe3+ on Aβ aggregation was investigated by two approaches: co-incubation and sequential addition. Our results using ex situ AFM, ThT-induced fluorescence, and FTIR spectroscopy indicated that the co-incubation of Cu2+, Zn2+, and Fe3+ significantly altered the morphology of aggregates. A concentration dependence study with mixed metal ions suggested that Zn2+ was required at much lower concentrations than Cu2+ to yield nonfibrillar amorphous Aβ deposits. In addition, sequential addition of Zn2+ or Cu2+ on fibrillar aggregates formed by Fe3+ demonstrated that Zn2+ and Cu2+ could possibly change the conformation of the aggregates induced by Fe3+. Our findings elucidate the coexistence of multiple metal ions through their interactions with Aβ peptides or its aggregates. [ABSTRACT FROM AUTHOR]

Abstract: Cells conditioned by repeated treatments with low doses of H2O2, were compared with its parental V79 cells for expression of ND1 and ND4 subunits of NADH dehydrogenase, a mitochondrial gene. It was found that ND1 and ND4 subunits were overexpressed in these conditioned cells. These cells were also found to be resistant to killing upon γ-irradiation through suppression of apoptotic cell death. On irradiation, the expression of both subunits decreased in both cell types, but overall there was more expression of both subunits in the conditioned cells. These findings indicate alteration in the expression of NADH dehydrogenase, a mitochondrial gene, could be involved in the recovery of γ-irradiated cells through inhibition of apoptosis. [Copyright &y& Elsevier]

Abstract: We have derived cells from the Chinese hamster V79 cell line by conditioning them with repeated low doses of hydrogen peroxide (H2O2). This mimics the physiological condition where cells are repeatedly exposed to low levels of oxidants. In an attempt to characterize such cells, we have exposed both conditioned cells (V79C) and the parental V79 cells (V79P) to different types of cytotoxic agents and compared their sensitivity to cell killing. The V79C cells were found to be stably resistant to killing by agents that produced toxicity through oxidative stress, e.g. H2O2 and cisplatin. It was also found that the lipid peroxidation produced by these agents were considerably lower in the V79C cells. Thus, the difference in sensitivity could be due to lesser extent of damage to these cells. V79C cells had greater antioxidant defense through higher GSH content and greater activity of enzymes such as Cu–Zn superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx), which provided protection from damage. Enzyme activities were also assayed at different times after treatment with various cytotoxic agents; there was a relatively large increase in SOD activity which perhaps plays a key role in determining the resistance of the V79C cells to killing. [Copyright &y& Elsevier]

Cancer is one of the major causes of death, and its negative impact continues to rise globally. Chemotherapy, which is the most common therapy, has several limitations due to its tremendous side effects. Therefore, developing an alternate therapeutic agent with high biocompatibility is indeed needed. The anti-oxidative effects and bioactivities of several different crude extracts of marine algae have been evaluated both in vitro and in vivo. In the present study, we synthesized the aqueous extract (HA) from the marine algae Amphiroa anceps, and then, a liposome was formulated for that extract (NHA). The extracts were characterized using different photophysical tools like dynamic light scattering, UV–visible spectroscopy, FTIR, scanning electron microscopy, and GC-MS analysis. The SEM image revealed a size range of 112–185 nm for NHA and the GC-MS results showed the presence of octadecanoic acid and n-Hexadecanoic acid in the majority. The anticancer activity was studied using A549 cells, and the NHA inhibited the cancer cells dose-dependently, with the highest killing of 92% at 100 μg/mL. The in vivo studies in the zebrafish model showed that neither the HA nor NHA of Amphiroa anceps showed any teratogenic effect. The outcome of our study showed that NHA can be a potential drug candidate for inhibiting cancer with good biocompatibility up to a dose of 100 μg/mL. [ABSTRACT FROM AUTHOR]

Flavonoids are natural polyphenolic compounds that mainly possess antioxidant properties due to more hydroxyl groups in their structure and play an important role in combatting many diseases. Myricetin is a flavonoid found in grapes, green tea, fruits, and vegetables and is not only an antioxidant but also is a pro-oxidant. Myricetin is sparingly soluble in water and restricts its properties due to low bioavailability. The present study reports the liposomal nanoformulations of myricetin to improve its bioavailability with reduced pro-oxidant activity. The nanoformulated myricetin was characterized using different photophysical tools, such as dynamic light scattering (DLS), zeta potential, and scanning electron microscopy (SEM). The effect of nanoencapsulated myricetin on the developing zebrafish embryo was studied in terms of microscopic observations, cumulative hatchability, and antioxidant activities, such as catalase, glutathione peroxidase, and superoxide dismutase, after treating the zebrafish embryo with standard oxidant hydrogen peroxide. The results obtained from the cumulative hatchability, developmental studies, and antioxidant assays indicated that the liposomal nanoformulation of myricetin had enhanced antioxidant activity, leading to defense against oxidative stress. The formulation was highly biocompatible, as evidenced by the cumulative hatching studies as well as microscopic observations. The positive effects of liposomal nanoformulation on zebrafish embryos can open an avenue for other researchers to carry out further related research and to check its activities in clinical studies and developmental studies. [ABSTRACT FROM AUTHOR]

Bupropion (Bup) belongs to the norepinephrine–dopamine reuptake inhibitor (NDRI) class and it is the only FDA-approved drug of its class for the treatment of major depressive disorder (MDD), sold under the name of Wellbutrin. Although bupropion is effective in suppressing the symptoms, its regular use and overdose might lead to seizures and liver failure. Thus, we aimed to nanoformulate bupropion onto a niosomal vesicle to improve its efficacy and achieve the same therapeutic effect at lower scheduled doses. A thin film hydration method was adopted to synthesize and optimize Bup entrapped niosomes using three different surfactants of the sorbitan ester series (Span 20, 40, and 60) in combination with cholesterol. The optimization data determined that the niosome formulated with a cholesterol-to-surfactant ratio of 1:1.5 is the most stable system, with the Bup entrapped niosomes containing Span 20 (Bup@N20C) exhibiting minimal in vitro and in vivo toxicity, and demonstrating the sustained release of Bup in artificial cerebrospinal fluid (ACSF). The Bup@N20C formulation showed increased exploration activity and reduced irregular movements in reserpine-induced depression in the adult zebrafish model, suggesting the potential for mood improvement through the suppression of depression-like behavior which was established by statistical analysis and trajectory data. The Bup@N20C-treated group even surpasses the treatment effect of the positive control group and is comparable to the control group. Hence, it can be inferred that niosomal formulations of Bup represent a promising delivery system capable of achieving the brain delivery of the cargo by bypassing the blood–brain barrier facilitated by their small architectural structure. [ABSTRACT FROM AUTHOR]

Various nanomaterials have been studied for their biomedical application in recent years. Among them, nanocomposites have a prominent medical application in the prevention, diagnosis, and treatment of various diseases. Nanocomposites are made up of polymeric matrix layers composed of synthetic or natural polymers like chitosan, polyethylene glycol, etc. Polymer nanocomposites are inorganic nanoparticles dispersed in a polymer matrix. There are two types of polymeric nanocomposites which include natural and synthetic polymer nanocomposites. These nanocomposites have various biomedical applications, such as medical implants, wound healing, wound dressing, bone repair and replacement, and dental filling. Polymeric nanocomposites have a wide range of biomedical applications due to their high stability, non-immunogenic nature, sustained drug delivery, non-toxic, and can escape reticuloendothelial system uptake along with drug bioavailability improvement. In this review, we have discussed various types of natural and synthetic polymer nanocomposites and their biomedical applications. [ABSTRACT FROM AUTHOR]

Alzheimer's disease (AD) is diagnosed with the deposition of insoluble β-amyloid (Aβ) peptides in the neuropil of the brain leading to dementia. The extracellular deposition of the fibrillar Aβ peptide on the neurons is known as senile plaques. Therefore, Aβ degradation and clearance from the human body is a promising therapeutic approach in the medication of AD. In the current study, the enzyme lumbrokinase (LK) was extracted and purified from earthworm and its activity was utilized toward Aβ 1–42 amyloids degradation in vitro alongside with an additional enzyme serratiopeptidase (SP) considering nattokinase (NK) as a standard. The output of this study revealed that preformed Aβ 1–42 amyloids was disintegrated by both LK and SP, as demonstrated from fluorescence assay using Thioflavin T dye. In addition, dynamic light scattering study revealed the lower size of the preformed fibrils Aβ 1–42 at various time intervals after incubation with the enzymes LK and SP. Furthermore, in silico approach showed high affinity thermodynamically favorable interaction of LK as well as SP toward Aβ 1–42 amyloid. Finally, the toxicity of degraded preformed Aβ 1–42 amyloid was assessed by MTT assay which showed reduced toxicity of enzyme treated Aβ 1–42 amyloid compared to only Aβ 1–42 amyloid. The findings of the present study indicated that LK and SP, not only had Aβ 1–42 amyloid degrading potential, but also could reduce the toxicity which can make them a suitable drug candidate for AD. Furthermore, the in vivo studies are needed to be executed in future. [ABSTRACT FROM AUTHOR]

Several formulations have been developed in the current era using liposomes and niosomes as vesicular carriers, which have proven useful in oral drug delivery; nevertheless, their use is limited due to their gastrointestinal environment, including pH, enzymes, and bile salts. To overcome these difficulties, researchers are working on finding ways to improve the efficacy and stability of vesicles. Therefore bilosomes have been developed as promising vesicular carriers with the potential to deliver oral vaccines, parenteral and transdermal targeted drug delivery. In addition to incorporating hydrophilic as well as lipophilic drugs into vesicles, bilosomes are considered one of the most effective methods for enhancing bioavailability and efficacy. Bile acid-based bilosomes are rapidly growing in the current research areas and are expected to provide multiple applications in the pharmaceutical and biomedical fields that will occur in the future with bile salts. This paper briefly introduces the bilosomes of a new generation (structure), their mechanism of action, stability, physicochemical properties, and potential biomedical applications including in oral immunization. Furthermore, surface-engineered bilosomes are more effective than bare bilosomes in various animal models, but clinical trials are needed to assess their safety and efficacy. There is also a need for more research on scaling-up factors for commercializing bilosomal systems. [ABSTRACT FROM AUTHOR]

Conventional chemotherapeutic drugs are used for cancer management, but recently nanoparticles have also been shown to contribute towards controlling cancer cell proliferation. In the present study, we focussed on analyzing the combinatorial effect of Cerium oxide (CeO 2) nanoparticles and Doxorubicin (Dox) on melanoma cancer cells in vitro and in vivo. We entrapped CeO 2 , Dox, and CeO 2 +Dox in a hybrid polymer matrix of alginate and chitosan (Alg-Cs) and used them in both in vitro and in vivo studies to compare their anticancer effect. Scratch assay using A549 lung cancer cells showed delayed wound healing when exposed to a low and high dose of CeO 2 +Dox, compared to individual components. In order to determine a safe dose of the nanoformulations, zebrafish embryos were used. Further, i n vivo, testing was done on Swiss albino female mice where the melanoma was induced by applying Benzopyrene followed by UV irradiation. The animals were treated with CeO 2 , Dox, and CeO 2 + Dox that were entrapped in Alg-Cs for further 21 days. From both in vivo and in vitro results, we concluded that CeO 2 and Dox in combination had superior therapeutic efficiency in cancer cells and animals than the nude drugs. [Display omitted] [ABSTRACT FROM AUTHOR]

There is significant progress in biomedical sciences to use biomaterials as a potential medium for the delivery of pharmacologically active components to diseased cells. This multidisciplinary approach has established that the therapeutic benefit is not directly proportional to the potency of drugs. It is more related to the mode of drug formulations and routes of administration. Biomaterials play a vital role in the formulations of a wide range of pharmaceutical compounds, including antibodies, peptides, drugs, enzymes, and vaccines. Most of these materials have been engineered to release therapeutics for an extended period to overcome the limitations of conventional therapies. This review has initially discussed a brief history of different biomaterials in drug delivery and the clinical needs of the same. The latter part describes the strategies to use RNA as a therapeutic molecule to stop the synthesis of disease-causing proteins that are generated by the misregulations. [ABSTRACT FROM AUTHOR]

Cascade molecules are nearly uniform-sized macromolecules of small molecules or linear polymer cores built around symmetric branching units. A wide range of biological properties can be achieved with phosphorus-containing dendrimers, depending on their terminal functions, ranging from biomaterials to imaging, drug delivery, and acting as a drug by themselves. This feature article presents significant examples of phosphorus-containing dendrimers used to develop biochips, support cell cultures, carry or deliver biomacromolecules and drugs, bioimaging, and combinational benefits. Because of the thermal stability, ferrocene function, and physical and chemical properties of phosphorus, dendrimers show greater rigidity, mobility, and strength. These dendrimers will be discussed as having a favorable effect on cell growths, especially on neuronal cells, as well as human immune cells like natural killer cells and monocytes, which have a crucial part in preventing cancerous and viral infections. Several phosphorus dendrimers are effective as drugs by themselves (drug per se) and show their activity against neurodegenerative diseases, cancer, inflammation, ocular hypertension, and transmissible spongiform encephalopathies (TSEs) in both in vivo and in vitro. The present review discusses the synthetic route, fabrications, and biomedical applications of phosphorus-containing dendrimers. The toxicity of these dendrimers was also reported. [ABSTRACT FROM AUTHOR]

The excellence of nanotechnology paved the way for its application in the food industry recently. Several industrial initiatives are now working on developing nano-based food packaging to improve food quality and ensure its safety. Along with providing improved mechanical property and barrier system, it also intimates the current condition of a food product. The ultimate goal is to extend the shelf life of food products, which the use of nanostructures can accomplish. The fabricated nanostructure is designed to release preservatives such as antimicrobials, at times to improve the shelf life. Two key applications of nanotechnology in the food sector are to develop nanostructured materials for food packaging or processing and nanosensors to detect food spoilage. This review discusses the types of nanomaterials used for food packaging, the advantages of nanobased packaging over conventional methods, and provides an overview of the risk of nanoparticles on the biological system. [ABSTRACT FROM AUTHOR]

Nanoparticles (NPs) designed for various theranostic purposes have hugely impacted scientific research in the field of biomedicine, bringing forth hopes of a future revolutionized area called nanomedicine. A budding advancement in this area is the conjugation of various cell membranes onto nanoparticles to develop biomimetic cells called 'Nanodecoys' (NDs), which can imitate the functioning of natural cells. This technology of coating cell membranes on NPs has enhanced the working capabilities of nano-based techniques by initiating effective navigation within the bodily system. Due to the presence of multiple functional moieties, nanoparticles coated with cell membranes hold the ability to interact with complex biological microenvironments inside the body with ease. Although developed with the initial motive to increase the time of circulation in the bloodstream and stability by coating membranes of red blood cells, it has further outstretched a wide range of cell lines, such as mesenchymal stem cells, beta cells, thrombocytes, white blood cells, and cancer cells. Thus, these cells and the versatile properties they bring along with them open up a brand-new domain in the biomedical industry where different formulations of nanoparticles can be used in appropriate dosages to treat a plethora of diseases. This review comprises recent investigations of nanodecoys in biomedical applications. [ABSTRACT FROM AUTHOR]

Biological events can be mapped in real-time using fluorescent images at high spatial resolution through the use of a powerful tool called fluorescence, and it is necessary to have ultra-bright fluorescent probes. The detrimental effects associated with the existing fluorescence imaging probes and contrast agents are the primary reason behind the greater involvement of nanotechnology. Developing advanced particles at the molecular and supramolecular levels is the only way to address the constraints underlying the current scenario. Nanosized structures dominate in multiple fields, especially in nanotheranostics, due to their higher quantum yield, negligible photobleaching, excellent biocompatibility, tunable optical properties, and improved circulation half-lives. Nanofluorophores, which are nanoparticles encapsulated or doped with fluorescent dyes, play a crucial role in fluorescence-based imaging modality by providing noninvasive realtime monitoring of the inner machinery of the anatomical and cellular structures. In addition to fluorescent inorganic and organic nanoparticles, there are labeled hydrophilic and hydrophobic nanostructures, semiconducting dots, carbon dots, as well as upconversion nanomaterials, etc., which are widely used in fluorescent imaging. A comprehensive literature survey has been provided in this review since intense studies are needed to clear the preclinic stage, thus opening up opportunities for future biomedical applications. [ABSTRACT FROM AUTHOR]

Photodynamic therapy (PDT) is a well-known remedial treatment for cancer, infections, and various other diseases. PDT uses nontoxic dyes called photosensitizers (PS) that are activated in visible light at the proper wavelength to generate ROS (reactive oxygen species) that aid in killing tumor cells and destroying pathogenic microbes. Deciding a suitable photosensitizer is essential for enhancing the effectiveness of photodynamic therapy. It is challenging to choose the photosensitizer that is appropriate for specific pathological circumstances, such as different cancer species. Porphyrin, chlorin, and bacteriochlorin are tetrapyrroles used with proper functionalization in PDT, among which some compound has been clinically approved. Most photosensitizers are hydrophobic, have minimum solubility, and exhibit cytotoxicity due to the dispersion in biological fluid. This paper reviewed some nanotechnology-based strategies to overcome these drawbacks. In PDT, metal nanoparticles are widely used due to their enhanced surface plasmon resonance. The self-assembled nano-drug carriers like polymeric micelles, liposomes, and metal-based nanoparticles play a significant role in solubilizing the photosensitizer to make them biocompatible. [ABSTRACT FROM AUTHOR]

In consideration of the issues of drug delivery systems, the artificial vesicle structures composed of block copolymers called polymersomes recently gained considerable attention. The possibility of tuning the mechanical parameter and increasing the scale-up production of polymersomes led to its wide application in healthcare. Bearing in mind the disease condition, the structure and properties of the polymersomes could be tuned to serve the purpose. Furthermore, specific ligands can be incorporated on the vesicular surface to induce smart polymersomes, thus improving targeted delivery. The synthesis method and surface functionalization are the two key aspects that determine the versatility of biological applications as they account for stability, specific targeting, degradability, biocompatibility, and bioavailability. A perfectly aligned polymer vesicle can mimic the cells/organelles and function by avoiding cytotoxicity. This supramolecular structure can carry and deliver payloads of a wide range, including drugs, proteins, and genes, contributing to the construction of next-generation therapeutics. These aspects promote the potential use of such components as a framework to approach damaged tissue while maintaining healthy environments during circulation. Herein, this article concentrates specifically on the drug delivery applications of polymersomes. [ABSTRACT FROM AUTHOR]

Medical imaging is currently revolutionizing the diagnosis and treatment of a variety of diseases. Several imaging modalities have been developed based on advances in science and engineering. The impact of these imaging tools has been further improved with the advent of various modern chemistries, leading to the development of contrast agents that serve further to localize the detection of diseased tissues. Several researchers are recently involved in engineering contrast agents that can generate contrast differences between tissues in multiple imaging modalities, enabling cross-referenced determination of anomalies. To establish these multimodal imaging agents, nanovectors have gained significance due to their key physicochemical properties. The major focus of this review is on the engineering strategies of nanovectors for multimodal medical imaging. The review conceives the basic principles, major parameters, and limitations of imaging modalities, namely, magnetic resonance imaging (MRI), computed tomography (CT), and fluorescence imaging at the beginning. Drawbacks of traditional contrast agents and the demand for new contrast agents are established. The importance of multimodal imaging and the need for a single contrast agent for these imaging applications are elaborated. Finally, the advantages, limitations, and design considerations of nanovectors based on magnetic and metallic nanoparticles with surface modifications to reduce toxicity and enable targeted delivery as multimodal imaging agents are also emphasized. [ABSTRACT FROM AUTHOR]

Abstract: In prion diseases, the posttranslational modification of host-encoded prion protein PrPc yields a high β-sheet content modified protein PrPsc, which further polymerizes into amyloid fibrils. PrP106–126 initiates the conformational changes leading to the conversion of PrPc to PrPsc. Molecules that can defunctionalize such peptides can serve as a potential tool in combating prion diseases. In microorganisms during stressed conditions, small stress molecules (SSMs) are formed to prevent protein denaturation and maintain protein stability and function. The effect of such SSMs on PrP106–126 amyloid formation is explored in the present study using turbidity, atomic force microscopy (AFM), and cellular toxicity assay. Turbidity and AFM studies clearly depict that the SSMs—ectoine and mannosylglyceramide (MGA) inhibit the PrP106–126 aggregation. Our study also connotes that ectoine and MGA offer strong resistance to prion peptide-induced toxicity in human neuroblastoma cells, concluding that such molecules can be potential inhibitors of prion aggregation and toxicity. [Copyright &y& Elsevier]

The protein misfolded structure called amyloids is related with extensive range of pathologies like local amyloidosis and neurodegenerative diseases. Several studies have reported the potential of insulin to generate local amyloidosis under certain state. Reports also showed that fibrils of insulin generated local amyloid mass due to continuous subcutaneous injection in mouse as well as rat. The present study was designed to examine the consequence of insulin fibril injections in rats, as well as the ability of enzymes, Lumbrokinase (LK) and Serratiopeptidase (SP) in diminishing this amyloid mass progression. The results showed that insulin fibrils generated amyloid masses in rats after subcutaneous injection for two weeks which was significantly condensed in size for the groups injected with insulin fibrils combined with LK or SP. At higher doses of LK and SP, the absence of amyloid structure was observed in histopathological studies. Light microscopy, polarized microscopy as well as Lumia live in vivo imaging system was used to analyze the results. In conclusion, the overall outcome of this study showed the anti-amyloid potential of enzyme LK and SP in the attenuation of local amyloidosis. Unlabelled Image [ABSTRACT FROM AUTHOR]

An electrokinetic potential (ζ-potential) based approach was introduced to address the amyloid degradation on ZnO-nanoflower platform. The hallmark of neurodegenerative disorders like Alzheimer's disease, Parkinson's disease (PD), Creutzfeldt-Jakob Disease (CJD), Prion- associated diseases, type-II diabetes, etc. is the deposition of misfolded protein aggregates predominantly β-sheeted in structure and fibrillar morphology, known as amyloids, in the brain and different parts of the body. Agents that can degrade these amyloids can be potential candidate for the therapy of amyloidosis. Ultrasmall nanoparticles are gaining interest due to their ability to cross blood brain barrier (BBB) which is favorable for the treatment of neurodegenerative disorders. Considering the influence of Zn2+ in the formation of Aβ aggregates instead of fibrillation, the present study was designed based on the ZnO nanoparticles (ZnO-NP) and ZnO nanoflowers (ZnO-NF) to compare the anti amyloid ability using a model huminsulin amyloid. Fluorescence study, atomic force microscopy (AFM), IR spectroscopy (FTIR) and reduction of fibril size using dynamic light scattering showed that ZnO-NF can degrade amyloids with a higher capacity than their nanoparticle counterpart. Significant reduction in magnitude of ζ-potential in ZnO-NF treated huminsulin amyloid supported the notion to come to the consensus and became the new indicator for anti-amyloidosis. The cell viability assay of ZnO-NP and ZnO-NF at a higher dose than that used for amyloid degradation using PC12 and HaCaT cell lines showed their biocompatibility in a safe manner. Thus, it can be suggested that ZnO-NF would be a better candidate for amyloid degradation compared to ZnO-NPs due to higher surface to volume ratio of the petals. Unlabelled Image • Amyloidosis requires degradation of amyloids as a potential therapy. • Agents that can degrade amyloids are potential drug candidates. • Zinc oxide nanoflower (ZnO-NF) structure was exploited to dissociate insulin amyloids in vitro. • A decrease in ζ-potential magnitude was used as a parameter for anti amyloid activity. • The engineered ZnO-NF was found to be non toxic. [ABSTRACT FROM AUTHOR]

Zinc oxide (ZnO) is a semiconductor metal oxide nanoparticle with inherent optical properties. Among the different zinc oxide nanostructures, nanoflowers have greater surface area. Utilizing this property a reagentless biosensor has been developed for the detection of beta amyloids, a hallmark of neurodegenerative diseases like Alzheimer's disease, Creutzfeldt-Jakob Syndrome, insulin dependent type II diabetes etc. The poor fluorescence quantum yield and photobleaching effect of Thioflavin T (ThT) upon binding to the model insulin amyloid beta sheets in solution can be overcome by the present engineered biosensor where ThT acts as a target as well as a reporter to detect amyloids adsorbed on a solid template based on ZnO nanoflower. ThT was adsorbed on ZnO NFs grown over nano-silver thin film coated glass slide. The in vivo imaging system was used to detect and quantify the fluorescence intensity generated from the substrates upon binding with insulin amyloid. ZnO NFs have the waveguiding property which increases the local field intensity caused by a resonance between the guided fundamental mode and evanescent field associated with high- order modes. This resonance phenomenon reinforces the excitation of the fluorophores in close proximity of the NFs thereby exhibiting enhanced fluorescence like Fabry Pero't Resonator (FPR). Considering the engineering and sensitivity, the reported nanobiosensor developed on ZnO nanoflower can be treated as faster and cost effective amyloid sensor. [ABSTRACT FROM AUTHOR]

Amyloidosis is a group of diseases caused by the accumulation of insoluble protein aggregates in different parts of the body. Repeated subcutaneous injection of insulin hormones in diabetic patients leads to localized amyloidosis that is found to be cytotoxic. Thus, agents that can dissociate these aggregates are critically needed. In the present study, insulin amyloid dissociation was demonstrated by the treatment of an enzyme lumbrokinase (LK) isolated from earthworm. Thioflavin T (ThT) fluorescence, solution turbidity, particle size analysis, FTIR, CD, atomic force microscopy and cell viability assay were employed to support the dissociation of insulin amyloid in vitro . The small animal optical imaging was used to explore the dissociation of amyloid fibrils in vivo using zebrafish model. The activity of LK towards amyloid dissociation was compared with the standard amyloid fibril degrading agent nattokinase (NK). Our results indicated that LK can be a probable fibril degrading agent for the dissociation of amyloids. [ABSTRACT FROM AUTHOR]

A transition of amyloidogenic protein by alternative folding pathway under certain conditions leads to the formation of protease resistant amyloid fibrils, having predominantly cross β structure. These amyloids are related to various neurodegenerative diseases and clearance of such amyloids may be a therapeutic approach for amyloid-related diseases. Insulin, that can form amyloids, is widely used as a model amyloidogenic protein for the study of various amyloid related diseases. In this study, insulin amyloids were formed in vitro and the potential of Serratiopeptidase (SP), a fibrinolytic-like serine protease, towards the dissociation of insulin amyloids was explored. The dissociation of the amyloids was demonstrated using in vitro and in vivo using zebrafish model. The amyloid dissociation property was compared with a standard amyloid dissociating enzyme nattokinase (NK). SP shows better amyloid dissociation ability than NK and therefore, SP can be considered as amyloid dissociating agent with potential as a drug candidate for different amyloid related disorders. [ABSTRACT FROM AUTHOR]

The present study shows the thorough investigations on optical properties and hydrodynamic diameters of glutathione (GSH) stabilized nanosilver clusters (AgNC) at different stages of synthesis and engineering for the optimized absolute quantum yield to generate fluorescent images of Dalton Lymphoma Ascites (DLA) tumour bearing mice. The initial increment of quantum yield was wavelength dependent and finally it became 0.509 which was due to the camouflaging or entrapment of AgNC in macrophages membranes. The potentiality of macrophages membrane camouflaged silver nanoclusters (AgM) was reflected in the cell viability assay and confocal based live dead cell assay where the AgM has better cell killing effect compared to AgNC with reduced dosage and in vivo mice imaging generated the clear visualization at the tumour sites. Therefore, from the present study, it can be considered that the camouflaged nanosilver can be used for targeted theranostic applications. [ABSTRACT FROM AUTHOR]