Search

This study aims to provide verification between measured and calculated radiation dose using three different ionization chamber detectors in Grid plans to select the best ones To the best of our knowledge, this is the first practical experiment in such subject. Grid radiotherapy is an unconventional method for bulky tumors treatment. It is characterized by a single-fraction and high radiation dose. Ten cases (scenarios) were selected to achieve Grid plans by MLCs, with a single dose of 1500-2000 cGy. Three ionization detectors were employed to measure the maximum, mean, and point doses (cGy), and match them with those calculated by the linear accelerator used in this study. The results showed significant differences among the three detectors in measuring the maximum and mean doses, with p-value = 0.0016 and 0.06, respectively. While the differences among the measured three detectors and calculated doses for the point dose were non-significant, p = 0.12. The variation in the results of the corresponding percentage between calculated and measured doses depended on the type and position of the detector, the scattering, and the leakage of the radiation. In conclusions, the Semi-flex chamber gives the best results.

One mechanism of ciprofloxacin resistance is attributed to chromosomal DNA-encoded efflux pumps such as the MepA and NorB proteins. The goal of this research is to find a way to bypass Staphylococcus aureus’ efflux pumps. Because of its high membrane permeability and low association with NorB and MepA efflux proteins, a liposome-encapsulating antibiotic is one of the promising, cost-effective drug carriers and coating mechanisms for overcoming active transport of methicillin-resistant S. aureus (MRSA) multidrug-resistant efflux protein . The calculated “Log Perm RRCK” membrane permeability values of 1,2-distearoyl-sn-glycerol-3-phosphocholine (DSPC) ciprofloxacin liposome-encapsulated (CFL) showed a lower negative value of − 4,652 cm/s and greater membrane permeability than ciprofloxacin free (CPF). The results of RT-qPCR showed that cationic liposomes containing ciprofloxacin in liposome-encapsulated form (CFL) improved CPF antibacterial activity and affinity for negatively charged bacterial cell surface membrane in comparison to free drug and liposome, as it overcame several resistance mechanisms and reduced the expression of efflux pumps. Ciprofloxacin liposome-encapsulated (CFL) is therefore more effective than ciprofloxacin alone. Liposomes can be combined with a variety of drugs that interact with bacterial cell efflux pumps to maintain high sustained levels of antibiotics in bacterial cells.

The present study aims to assess natural radioactivity and its radiological hazards and dose parameters in granite waste samples. These wastes arise through uranium chemical leaching, then they were scrutinized by gamma ray spectrometry (HPGe detector) the concentration of U-238 samples ranged between (556 and 1479) Bq/kg, Th-232 ranged between (18 and 690) Bq/kg, Ra-226 samples ranged between (911and 2269) Bq/kg and K-40 ranged between (461 and 675) Bq/kg. Radon daughter and airborne dust are safe. The annual effective dose equivalent was 0.2 mSv/y. In conclusion we recommended reusing these waste in paving roads in open places.

Background Liposomes have the ability to enclose hydrophilic or lipophilic materials. Bioactive macromolecules become more stable when they are entrapped within liposomes resisting environmental changes, allowing maintenance of the antimicrobial molecules and increasing their effectiveness and constancy thus can be used for food preservation. The aim of this study was to screen food samples for microbial contamination and to examine the antimicrobial activity of selected six ready-made plant oils which were; clove, black seed, thyme, garlic, rosemary and green tea against the isolated microbes from food samples and other selected microbes. Also to examine the possible enhancement of the antibacterial property of clove oil and tetracycline versus Escherichia coli when they were encapsulated into distearoyl phosphatidylcholine (DSPC) liposomes as a nanoscale carriers. Results of the antimicrobial action measured by minimum inhibitory concentration revealed that all six oils had antimicrobial action when facing at least one of the tested microbes. However only clove oil could inhibit the growth of all tested microbes. Moreover encapsulation of clove oil into DSPC liposomes enhanced its antibacterial action by 10 times when examined to inhibit the growth of E. coli. Also the antibacterial activity of liposome encapsulated tetracycline was improved by 8 times. Results of characterization of formulated clove oil liposomes by measuring their Zeta potential and their sizes implying that clove oil might be enclosed within the hydrophobic portion of the two layers of the liposome. Analyzing data of Fourier Transform Infrared Spectroscopy showed that clove oil was detected in the interfacial area of the liposome. Analyzing results of Differential scanning calorimetry and measuring phase transitions suggested that liposomes encapsulating clove oil had a membrane fluidization effect. Conclusion Some plant oils like clove has antimicrobial activity which enhanced with liposomal encapsulation and thus reduces the needed concentration to give the desired actions.

Coronavirus diseases 2019 (COVID-19) are seriously affecting human health all over the world. Nucleotide inhibitors have promising results in terms of its efficacy against different viral polymerases. In this study, detailed molecular docking and dynamics simulations are used to evaluate the binding affinity of a clinically approved drug, sofosbuvir, with the solved structure of the viral protein RNA-dependent RNA polymerase (RdRp) and compare it to the clinically approved drug, Remdesivir. These drugs are docked onto the three-dimensional structure of the nsp12 protein of SARS-CoV-2, which controls the polymerization process. Hence, it is considered one of the primary therapeutic targets for coronaviruses. Sofosbuvir is a drug that is currently used for HCV treatment; therefore, HCV RdRp is used as a positive control protein target. The protein dynamics are simulated for 100 ns, while the binding is tested during different dynamics states of the SARS-CoV-2 RdRp. Additionally, the drug-protein complexes are further simulated for 20 ns to explore the binding mechanism. The interaction of SARS-CoV-2 RdRp as a target with the active form of sofosbuvir as a ligand demonstrates binding effectiveness. One of the FDA-approved antiviral drugs, such as sofosbuvir, can help us in this mission, aiming to limit the danger of COVID-19. Sofosbuvir was found to bind nsp12 with comparable binding energies to that of Remdesivir, which has been reported for its potential against COVID-19 RdRp and is currently approved by the FDA. Graphic abstract

In order to improve liposomal doxorubicin stability, differentiation between Heparin and Polyethylene Glycol (PEG) as biofunctionalization for liposomal doxorubicin has been investigated by measuring the entrapment efficiency, size distribution, zeta potential, evaluating the in vitro potential cytotoxicity against MCF-7 (Breast cancer cell) and stability in serum by measuring the drug release rate. We synthesized Four liposomal formulations: (A) Conventional liposomes; DPPC:DOX, (B) Positively charged PEGylated liposomes; DPPC:CHOL:SA:PEG:DOX (C) Negatively charged PEGylated liposomes: DPPC:CHOl:DCP:PEG:DOX (D) positively charged liposomes to conjugate heparin; DPPC:CHOL:SA:DOX. Entrapment efficiency of doxorubicin dramatically increased after PEGylation and conjugation with heparin. In addition, zeta potential was changed upon the encapsulation of doxorubicin into conventional and PEGylated liposomes which indicates that DOX encapsulated completely into liposomes. For heparin conjugated liposomes, zeta potential was slightly changed. Sulphorhodamine-B (SRB) assay showed a greater cytotoxic effect of the liposomal doxorubicin formulations at different concentrations with respect to free drug against MCF-7 cell lines. The anticancer activity order was observed between the various liposome formulations, especially those observed with conjugated heparin liposomes. Slower drug release rate showed an order of D > C > B > A that means stability showed an order of D > C > B > A. From above results, the most stable liposomal doxorubicin formulation was the liposomal formulation D. The results optimized using heparin than PEG as biofunctionalization. Further studies are suggested for better understanding why heparin improves the stability of liposomal doxorubicin.

Prodigiosins have been shown to have anticancer activities. 5-Fluorouracil (5-FU) is broadly used chemotherapeutic drug that treats different solid tumors including breast cancer but has low response rates and a variety of side effects. In this study, we evaluated the anticancer properties of prodigiosins in a murine model "Ehrlich tumor" and tested whether it can be added to 5-FU to potentiate its effects. Markers of oxidative stress; MDA, NO, and GSH levels were evaluated as well as antioxidant enzyme activities of CAT SOD, GR, and GPx. The levels of Bax, Bcl-2, PCNA, and NF-κB proteins were measured using ELISA kits. The mRNAs of p53 and Cdc2 and Casp3 were quantitatively measured by real-time PCR and ELISA respectively. Cell cycle analysis was performed using flow cytometery. Prodigiosins did not influence tumor volume. Prodigiosins have not induced oxidative stress while 5-FU did increase MDA, NO but decreased GSH levels. The combination prodigiosins and 5-FU did reduce oxidative stress markers; MDA, NO and increased GSH levels. Prodigiosins significantly increased CAT only while 5-FU did decreased SOD, CAT, GPx, and GR. The combination prodigiosins and 5-FU increased the levels of these enzymes again. Prodigiosins increased the Bax/Bcl-2 ratio while the combination deceased it. In conclusion, prodigiosins have pronounced anticancer properties but their combination with 5-FU decreased oxidative stress exerted by 5-FU but weakened the apoptotic effects of 5-FU. Prodigiosins could affect a key mechanism through which 5-FU exerts its tumor inhibitory effects.

We investigated the combinatorial cytotoxic actions of the chemotherapeutic drug (sorafenib tosylate, ST), in synergism with γ-radiation, on human hepatocellular carcinoma (HepG2) cells. The novel radiosensitizer, hexagonal gold nanoparticles (HG), was prepared and utilized to enhance the radiobiological response of HepG2 cells. A well-designed nanoporous alginate/calcium carbonate hybrid (ALG-CaCO3) was prepared as a biocompatible/biodegradable nanocarrier for co-delivery of the hydrophobic drug (ST) and the hydrophilic radiosensitizer (HG) to the cancer cells. Incubation of HepG2 cells with the prepared nanoprobes followed by irradiation with different doses (0, 3 or 6 Gy) of γ-radiation resulted in a significant reduction of the cells viability as a result of the synergistic (chemo-radiation) cytotoxic actions.

This work aims to evaluate cyclophosphamide (Cyclo) cytotoxic efficacy combined with liposomes in the presence or absence of beta carotene (beta) by detecting the effects of these compounds on the breast cancer cell line (MCF-7) DNA damage. The IC50 value for beta in cytotoxic assay with MCF-7 treated cells was 21.15 μg/ml, while with liposomal beta (LipoBeta) being 121 μg/ml. The free Cyclo IC50 value was 719.86 μg/ml, its liposomal form (LipoCyclo) was 172 μg/ml. The results indicated that in contrast with Cyclo and control values, all comet assay parameters for the LipoBeta were significantly increased (P < 0.05). In MCF-7 cells treated with beta, the findings show a higher intensity of comet tail than those treated with LipoBeta. The presence of several double-strand breaks suggests this high intensity relative to the head. The molecular combination between Cyclo and liposomes in the presence or absence of beta was characterized. Dynamic light scattering measurements confirmed the mono-dispersity of all samples. The incorporation of Cyclo or beta into liposomes exhibited a slight shift to higher temperature compared to the main peak of empty liposomes that exists at 101.5°C which creates a conformational disorder within the phospholipids. The FTIR study showed structural alterations in vesicles after liposome encapsulation.

Biocompatible cross-linked chitosan nanoparticles comprising the cancer chemotherapeutic drug (mitoxantrone, MX) and the novel radiosensitizer hexagonal gold nanoparticles (HG) were prepared and characterized. The prepared nanoparticles were applied, in synergism with external γ-radiation, as dual (chemo-radio) model for treatment of human breast cancer cell (MCF-7). In vitro studies revealed that HG significantly enhances the response of MCF-7 to low and moderate doses of γ-radiation (2 and 4 Gy). Cell viability assay demonstrated the synergistic anticancer actions of mitoxantrone chemotherapy and gold-sensitized γ-radiation therapy. The prepared combinatorial model is potential for efficient and safer treatment of MCF7 cancer cells.

Hypoxia is a condition in which proliferating tumor cells are deprived of oxygen due to limited blood supply from abnormal tumor microvasculature. This study aimed to investigate the molecular changes that occur in tumor cell hypoxia with special emphasis placed on the efficacy of chemotherapeutic and radiation-related effects. Four commercially available chemotherapeutic agents: cisplatin, cyclophosphamide, doxorubicin, and 5-fluorouracil, were tested for their cytotoxic activity on the cancer cell lines PC3 (prostate), HepG2 (liver), and MCF-7 (breast). Tumor cell lines under hypoxia were treated with both IC50 concentrations of the different chemotherapeutic agents and irradiated with 5 and 10 Gy using a 137Cs gamma source. Hypoxia-inducible factor-1α (HIF-1α) protein levels were examined using an ELISA assay. Hypoxic cells showed a significant change in cell viability to all chemotherapeutic agents in comparison to normoxic controls. HepG2 cells were more resistant to the cytotoxic drug doxorubicin compared to other cancer cell lines. The flow cytometric analysis showed that hypoxic cells have lower levels of total apoptotic cell populations (early and late apoptosis) compared to normoxic cells suggesting decreased hypoxia-induced apoptosis in cancer cells. The highest reduction in HIF-1α level was observed in the MCF-7 cell line (95.5%) in response to the doxorubicin treatment combined with 10 Gy irradiation of cells. Chemoradiotherapy could result in minimal as well as a high reduction of HIF-1α based on cell type, type of chemotherapy, and amount of ionizing radiation. This study highlights future research work to optimize a combined chemoradiotherapeutic regime in individual cancer cell hypoxia.

One mechanism of ciprofloxacin resistance is attributed to chromosomal DNA-encoded efflux pumps such as the MepA and NorB proteins. The goal of this research is to find a way to bypass Staphylococcus aureus' efflux pumps. Because of its high membrane permeability and low association with NorB and MepA efflux proteins, a liposome-encapsulating antibiotic is one of the promising, cost-effective drug carriers and coating mechanisms for overcoming active transport of methicillin-resistant S. aureus (MRSA) multidrug-resistant efflux protein . The calculated "Log Perm RRCK" membrane permeability values of 1,2-distearoyl-sn-glycerol-3-phosphocholine (DSPC) ciprofloxacin liposome-encapsulated (CFL) showed a lower negative value of - 4,652 cm/s and greater membrane permeability than ciprofloxacin free (CPF). The results of RT-qPCR showed that cationic liposomes containing ciprofloxacin in liposome-encapsulated form (CFL) improved CPF antibacterial activity and affinity for negatively charged bacterial cell surface membrane in comparison to free drug and liposome, as it overcame several resistance mechanisms and reduced the expression of efflux pumps. Ciprofloxacin liposome-encapsulated (CFL) is therefore more effective than ciprofloxacin alone. Liposomes can be combined with a variety of drugs that interact with bacterial cell efflux pumps to maintain high sustained levels of antibiotics in bacterial cells.

Aim: Lutein is a potent antioxidant that is found in ocular tissue. It protects retina against oxidative stress. We aimed to increase lutein efficiency by encapsulating it into liposome and...

The aim of the study was to correct for partial volume effect in positron emission imaging studies which is the most influential factors using three-dimensional (3D) representation of the recovery coefficients (RCs) to improve standardized uptake value (SUV) calculations. Several phantom studies were conducted at significantly wide range of lesion contrast, range 2:1 up to 15:1. It was then classified into two groups: one for generating 3D function taking into consideration the sphere size as well lesion contrast whereas the other group was used for functions validation. A segmentation threshold algorithm for lesion delineation and volume determination was generated based on lesion contrast and lesion size. In addition, five 3D functions of the RC of the SUV were formulated considering lesion size and lesion contrast. Validation of the new algorithms has considered both phantom and clinical studies. The error in threshold 3D function was well below 10%. For lesions ≤ 2 cm in diameter, there was no statistical difference of the functions developed for SUVmax as well as those functions generated for SUVmean. However, the median SUVmax has increased significantly when compared with data before correction. For SUVmean, the increase in median value was also significantly high. It has been successful to generate 3D mathematical formulations of the SUV RC taking into consideration the most influential factors including lesion size and lesion contrast. Validation studies were suggestive of the good performance of the new mathematical algorithms generated to correct for PVE. However, further studies are underway to ensure the performance of the proposed algorithms in clinical PET studies.

The goal of this study to investigate the influence of antioxidant as coenzyme Q10 on structural changes of model lipid membranes as DPPC by using Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). The results obtained indicate that the greater effect of CoQ10 upon the incorporation into negatively charged liposomes in comparison with the other liposome formulations. The incorporated CoQ10 is probably associated with the lipid bilayers, interacted to a large extent with them, and perturbed them which results in the strong broadening and shift to lower temperature 94 °C of the major characteristic endothermic peak of pure DPPC that exists at 105 °C. The FT-IR spectra of samples showed that Incorporation of CoQ10 into neutrally, positively and negatively charged DPPC liposomes showed significant change in the frequency of the antisymmetric CH2 stretching bands in the acyl chain implying that CoQ10 create a conformational disorder within the acyl chains of phospholipids. In other words, it had significant effect on the order of the membrane.

Purpose: To stress the influence of Coenzyme Q10 (CoQ10) on the structural properties of liposomes as model membranes and to investigate the possible role of CoQ10 or CoQ10 doped in liposomes when topically instilled as eye drops, in preventing cataract. Methods: The molecular interaction between liposomes and Coenzyme Q10 was examined using differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). Rat pups were randomly divided into six groups comprising 15 pups. Group (1), control group. Group (2), untreated model of cataract, received a single subcutaneous injection of sodium selenite. Instillation of pure CoQ10 (Group 3), CoQ10 encapsulated into neutral (Group 4), positive (Group 5) and negative (Group 6) Dipalmitoyl phosphatidylcholine (DPPC) liposomes on the opacification of lenses in rat pups after sodium selenite injection was topically received. Results: The incorporated CoQ10 is probably associated with lipid bilayers where it interacts to a large extent and perturbs them. This results in strong broadening and shift to lower temperature (94°C) of the major characteristic endothermic peak of pure DPPC at 105°C. FTIR showed that the incorporation of CoQ10 into DPPC induces a conformational change in the polar region of DPPC. Ophthalmological and Biochemical studies revealed that CoQ10 alone followed by negatively charged liposomes doped with CoQ10 are more effective in reducing the progress of cataract as well as improving the lens soluble proteins levels and total antioxidant capacity. Conclusion: The interactions of CoQ10 with membrane systems may contribute to a better understanding of CoQ10 physiological properties and the development of therapeutically advanced systems.

The present study investigated the efficacy of cationic liposome-encapsulated carotenoids (lutein or beta-carotene) as a treatment in an animal model of fibromyalgia (FM). Preparation and characterization of the nano-sized cationic liposomal carotenoids have been carried out. FM has been induced in the experimental animals via successive subcutaneous reserpine injection (1 mg/kg). Animals were divided into four groups; control, reserpinized (Res), reserpinized and cationic liposomal lutein-treated (Res + CL-Lut), and reserpinized and liposomal beta-carotene-treated (Res + CL-Bc). Levels of norepinephrine (NE), dopamine (DA), and serotonin (5-HT), and oxidative stress markers (MDA, H2O2, NO, and GSH) were determined in the brain's cortical tissue of the different groups of animals. Furthermore, the spectral analysis of the electrocorticogram (ECoG) was carried out. Animal behavior was tested for different animal groups. Results showed a significant reduction in monoamines, an elevation of oxidative stress markers, a shift in the ECoG frequency band power, and a change in pain threshold of the reserpinized animals. A return to a non-significant difference from the control values of all the measured parameters has been obtained after two weeks of cationic liposomal carotenoid preparations treatment. The present findings shed more light on the validity of the reserpine model of FM and provide evidence for the antidepressant, antioxidant, and anti-nociceptive potential of the cationic liposomal carotenoids. The present results proofed that the natural product preparations on a nano-sized scale could be a good alternative to the pharmacological interventions for FM treatment.

Technetium-99m is a radioactive tracer that emits gamma rays. Its half-life time is 6 h. Similar to other ionizing radiations, the main mechanism of radiation-induced effects is initiated through the production of reactive oxygen species (ROS). This study was designed to determine the possible protective effects of Ginkgo biloba and Angelica archangelica against oxidative organ damage that was induced byThe experiments were performed on thirty-six Wistar-rats which were subdivided into control groups and groups exposed toThere were no significant difference between the pre-treated and irradiated G. biloba group and control group, while both groups were significantly different (p .05) from the untreated irradiated group. On the other hand, treatment with A. archangelica did not confer any significant protection againstThis study demonstrated that G. biloba, through its free radical scavenging and antioxidant properties, successfully attenuated

This study assessed the use of

This work aims to investigate the effect of X-rays on poly(vinyl alcohol) (PVA) films and studying the ability to be a model of a synthetic cell membrane when compared to liposomes as biological models. The influence of X-ray irradiation on thin films of PVA doped with safranin (SAF) dye and liposomes encapsulated by SAF dye is studied using UV–visible spectrophotometry. These films are exposed to X-ray radiation with accumulated doses range of 10–50 Gy of 140 kVp at a constant dose rate of 2002 μGy/s. The absorption spectra of the PVA/SAF and the liposomes/SAF are measured. The absorption spectra of the PVA/SAF showed a decrease in the absorbance band peak with the increase of the dose with values are similar to those observed with the liposomes/SAF. The dose response function indicates the same radiation sensitivity of both samples. The results indicated that full width at half maximum of SAF/PVA and SAF/liposomes show linear decrease with an increase of dose. The variation in dose response is relatively small and found to be within 3.5% and the variations in a decrease of the absorbance peak are found to be with maximum 5%. These values can indicate that both of SAF/PVA and SAF/liposomes have the same behavior under the applied X-ray dose range. The results viewed that the PVA doped with SAF dye behave similarly as the liposomes doped with SAF dye. PVA may be used as a synthetic model for a cell membrane for probing X-ray-membrane interactions.

Nanofibrous mats were fabricated through blending of a synthetic polymer, polycaprolactone (PCL), and a natural one, gelatin (GT), using an electrospinning technique. Bicomponent of polycaprolactone/gelatin (PCL/GT) nanofibers was successfully formed by using acetic acid/formic acid (AA/FA) solvent system. In the present study the working parameters were studied to understand the conversion of polymer solutions into nanofibers through electrospinning. Various experimental parameters, such as solution concentration, applied voltage, distance between the tip and collector and solvent ratio, were studied. Each of those parameters can affect the fibers morphologies and diameter and by proper control of those parameters we can fabricate electrospun fibers with desired morphologies and diameters. It was found that the adequate conditions for PCL/GT nanofibers electrospinning were detected for 18%wt concentration and 18 kV applied voltage at tip to collector distance of 12 cm at solvent ratio 90:10 of AA/FA.

Eye drops account for 90% of ophthalmic formulations despite of the rapid precorneal drug loss. Our aim is to test the effect of positive charge induction and the subsequent size reduction on the efficiency of liposomes as ocular drug delivery system for the lipophilic drug prednisolone acetate (PSA). Different formulations of PSA-loaded liposomes, positive multilamellar liposomes (pMLV), positive small (nano-sized) unilamellar liposomes (pSUV) and neutral multilamellar liposomes (nMLV), were prepared. These formulations were characterized by measuring surface charge, size distribution, entrapment efficiency, release rate, and ability to deliver PSA across the cornea. In vitro studies showed that positive charge induction reduces the transcorneal flux (about 1.9-fold lower than nMLV), while the subsequent size reduction results in higher flux (about 1.2-fold higher than nMLV). But in vivo results revealed that pSUV produced more concentrations of PSA in aqueous humor than nMLV (P < 0.05) suggesting greater chance for drug penetration, pSUV were more effective than nMLV in this regard (P < 0.05). As revealed by in vivo studies and ophthalmic examinations, positive charge induction and the subsequent size reduction increased the efficiency of liposomes as ocular drug delivery system for PSA.

The main aim of the work was the fabrication of novel silver releasing nanocomposite scaffolds, for bone treatment, by the gas foaming/particulate-leaching technique. Silver doped bioactive glass nanoparticles were used as a filler, to provide the scaffolds with bioactivity, as well as anti-bacterial properties. Nanocomposite scaffolds containing 0, 20 and 40 wt% glass contents were prepared and coded as PAg0, PAg20 and PAg40, respectively. The scaffolds were characterized by SEM/EDXA, FTIR and TGA. Examination of SEM microphotographs showed that, the produced scaffolds had well interconnected structures. For PAg0, PAg20 and PAg40, the maximum pore sizes were about 250, 150 and 100 μm, respectively, while their porosities % were 92%, 89% and 83%, respectively. Degradation studies were carried out, by incubating the scaffolds in simulated body fluid, for a month. Results revealed the possibility to modulate and improve the degradation of the scaffolds by increasing their glass contents. The final weight losses measured for PAg0, PAg20 and PAg40 were 12.76%, 14.61% and 17.42%, respectively. On the other hand, the highest water absorption values recorded for those scaffolds were 61.89%, 240.36% and 270.87%, respectively, indicating that, the addition of glass nanoparticles to the scaffolds improved their water absorption abilities. Both PAg20 and PAg40 induced an apatite layer on their surfaces, had anti-bacterial effect in agar plates, and their silver releasing profiles followed a diffusion-controlled mechanism. Therefore they could be used for bone treatment.

The interaction between doxorubicin (DOX), an anthracycline antibiotic frequently used in chemotherapy, and zwitterionic dipalmitoylphosphatidylcholine (DPPC) was investigated using Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), and rheological measurements. FTIR results showed that DOX shifted the wavenumber of the PO(2)(-) band for pure DPPC to a higher wavenumber. This may have been because of the strong interactions between the NH(3)(+) group in DOX and the phosphate (PO(2)(-)) group in the polar head of DPPC. The main transition temperature of DPPC liposomes was slightly shifted to a lower temperature for DPPC liposome-encapsulated DOX. This suggested that DOX had a significant effect on the acyl chains in the DPPC bilayers, and that its presence decreased the transition cooperativity of lipid acyl chains. There was also the appearance of an additional transition peak at nearly 136 °C for the DPPC/DOX sample. These interactions between DOX and DPPC phospholipid would cause a decrease in the DPPC liposomes plastic viscosity and increase membrane fluidity. A better understanding of the interactions between DOX and lipid bilayers could help in the design and development of improved liposomal drug delivery systems.

Increased intraocular pressure (IOP) is a significant risk factor for the development of glaucoma. Timolol maleate is a beta-adrenergic receptor blocking agent and it is used for the treatment of glaucoma in order to reduce the elevated IOP that is characteristic of this eye disease. Systemic toxicity from topical timolol occurs more frequently than local toxicity and can affect the pulmonary, cardiac and central nervous systems. The objective of the present study, therefore, was to formulate multilamellar vesicles (MLVs) liposomal preparations of timolol maleate using their advantage of being less toxic compared with non-liposome-based drugs to be applied topically and to evaluate the in vivo performance of the prepared liposomes to extend the time of reduced IOP of glaucomatous rabbit's eye measured using a standard Shiotz tonometer. The encapsulation efficiency of MLVs was measured using a spectrophotometric technique. Differential scanning calorimetry (DSC) was used to monitor the effects of timolol maleate in the absence and presence of cholesterol on liposome thermal behaviour. Positively charged MLVs of timolol in the presence of a lower amount of cholesterol (DPPC(7):Chol(2):Timolol(2):SA(1) molar ratio) were found to be superior compared with other formulations in extending the ocular hypotensive effect approximately for 1 week (160 h) which encourages its physiological effectiveness. The increase of the cholesterol molar ratio in the prepared liposomal formulations serves to decrease the permeability of the lipid bilayer that is manifested by a low rate of drug release, an increased percentage of entrapment efficiency and a consequently lower bioavailability.

Objective To evaluate the effects of liposome-bound tetracycline eye drops in a rabbit dry eye model evaluating their advantage of being less allergic, preservative free and prolonged action compared with other tear substitutes. Procedures New Zealand albino rabbits were equally divided into control group and dry eye induced groups. Dryness was induced in 24 eyes of 12 healthy adult male albino rabbits by instilling atropine sulfate eye drops 1% three times daily for 1 week, then animals were subdivided into four groups; group 1 (rabbits with dry eye model), groups 2, 3, and 4: rabbits with dry eye model treated for 7 days starting on 7th day of dryness induction with either tetracycline, empty liposome, or combined tetracycline with liposome as topical eye drops respectively. Schirmer (STT) test and tear break up time (TBUT) were assessed on days 0, 2, 4, 7, 9, 11, and 14. Animals were sacrificed on day 14 and histopathological examination of the cornea and conjunctiva was performed. Results Tear break up time and STT test values were significantly improved in groups 2, 3, 4 as compared with group 1. The histopathological examination showed normal cytoarchitecture of corneas and conjunctivae in groups 2, 3, 4 against the dryness effect that continued to affect the cornea and conjunctival epithelium in group 1. There was a significant improvement in the group treated with liposome-bound tetracycline eye drops (group 4) as compared with tetracycline alone (group 2) and empty liposome (group 3). Conclusion The use of liposome encapsulated tetracycline significantly improved STT and TBUT values as well as reverse surface ocular pathology.

Nanoscales thermosensitive liposomes (TSL) composed of synthetic lipids (dipalmitoylphosphatidylcholine, and distearoylphosphatidylcholine), were used for doxorubicin encapsulation with 70% encapsulated efficiency. The liposomes were characterized by dynamic light scattering, transmission electron microscopy and turbidity method. Additionally, the liposomes exhibited a significant release of doxorubicin (Dox) by 60% within 5 min at 42°C. To assess the therapeutic efficacy of Dox in combination with hyperthermia, Dox free and encapsulated TSL were administered directly to Ehrlich tumor bearing mice at 1 mg/kg dose. Immediately after the drug administration, hyperthermia was applied to mention the temperature inside the tumor site at 42°C either for 5 min and 30 min. The results indicate a significant increase in the percent of apoptotic and necrotic cells in the treated group. Moreover, disrupts the integrity and the amount of intact DNA in tumor cells. In conclusion, Dox and hyperthermia may serve as a useful targeted drug delivery system for management of Ehrlich carcinoma.

Purpose: The aim of this study was to study the effect of ionizing radiation on apoptosis-related protein concentrations as well as the radio-protective role of Ginkgo biloba and Angelica archangelica. The experiments were performed on 68 adult Wistar rats weighing 175 g (±10 g). Animals were subdivided into control group in which the animals received neither the protector nor the isotopes. The second group represents the animals that received 1 mCi of 99mTc only. The third group represents the animals that received A. archangelica for 7 days. The fourth group represents the animals that received G. biloba for 7 days. The fifth group represents the animals that received 1 mCi of 99mTc once after receiving A. archangelica for 7 days. The sixth group represents the animals that received mCi of 99mTc once after receiving G. biloba for 7 days. Radiation was administered as intravenous injection by 1 mCi of 99mTc with the legend methoxyisobutylisonitrile for 24 h. The concentration of p53, Bcl2 and malondialdehyde in liver as well as histopathological examination of liver cells were carried out. Results showed that apoptotic to anti-apoptotic protein ratio significantly ( p < 0.05) returned to its normal ratio when radioisotopic injection was administered after the protection period for a week by both A. archangelica and G. biloba in a dose based on the animal body weight. Electron microscope photographing supported this finding. Conclusion: It was concluded that both antioxidants can be used as radio-protective agents in cases of ionizing radiation exposure.

To evaluate the effects of liposome-bound tetracycline eye drops in a rabbit dry eye model evaluating their advantage of being less allergic, preservative free and prolonged action compared with other tear substitutes.New Zealand albino rabbits were equally divided into control group and dry eye induced groups. Dryness was induced in 24 eyes of 12 healthy adult male albino rabbits by instilling atropine sulfate eye drops 1% three times daily for 1 week, then animals were subdivided into four groups; group 1 (rabbits with dry eye model), groups 2, 3, and 4: rabbits with dry eye model treated for 7 days starting on 7th day of dryness induction with either tetracycline, empty liposome, or combined tetracycline with liposome as topical eye drops respectively. Schirmer (STT) test and tear break up time (TBUT) were assessed on days 0, 2, 4, 7, 9, 11, and 14. Animals were sacrificed on day 14 and histopathological examination of the cornea and conjunctiva was performed.Tear break up time and STT test values were significantly improved in groups 2, 3, 4 as compared with group 1. The histopathological examination showed normal cytoarchitecture of corneas and conjunctivae in groups 2, 3, 4 against the dryness effect that continued to affect the cornea and conjunctival epithelium in group 1. There was a significant improvement in the group treated with liposome-bound tetracycline eye drops (group 4) as compared with tetracycline alone (group 2) and empty liposome (group 3).The use of liposome encapsulated tetracycline significantly improved STT and TBUT values as well as reverse surface ocular pathology.