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Abstract Poly l(+) lactic acid (PLLA) has become crucial in the biomedical industry for various uses. The direct polycondensation method was used to prepare Poly l(+) Lactic Acid (PLLA). Different catalysts, including metal oxides and metal halides, were used to test the polymerization technique. The effect of the amount of catalysts and the type of coupling agent were investigated. The effect of reaction time and polymerization solvents was also studied. PLLA was loaded with isosorbide dinitrate utilizing the solvent evaporation process. The synthesized polymer-drug system was evaluated by different means such as FT-IR, TGA, DSC, XRD, entrapment efficiency (E.E), drug loading (D.L), particle size analysis, and zeta potential determination. Studies on in-vitro release using UV light at 227 nm at various pH levels were conducted, and the kinetics of release and cytotoxicity using the sulforhodamine B (SRB) assay on human skin fibroblast cells were examined.

Rabab Kamel,1 Nahla A El-Wakil,2 Nermeen A Elkasabgy3 1Pharmaceutical Technology Department, National Research Centre, Cairo, Egypt; 2Cellulose and Paper Department, National Research Centre, Cairo, Egypt; 3Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, 11562, EgyptCorrespondence: Nermeen A ElkasabgyFaculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, EgyptTel +20 1141404144Email nermeen.ahmed.elkasabgy@pharma.cu.edu.eg; nermeenadelahmed@outlook.comPurpose: TEMPO-oxidized nanofibrillated cellulose (TONFC) originating from an agricultural waste (sugar cane) was utilized to prepare injectable in-situ forming hydrogel scaffolds (IHS) for regenerative medicine.Methods: TONFC was prepared and characterized for its morphology and chemical structure using TEM and FT-IR, respectively. The cold method was applied to prepare hydrogels. Various concentrations of poloxamer 407 were added to the prepared TONFC (0.5%w/w). Different sources of calcium, Fujicalin® (DCP) or hydroxyapatite (TCP), were used to formulate the aimed calcium-enriched raloxifene hydrochloride-loaded IHS. Gelation temperature, drug content, injectability and in-vitro drug release were evaluated along with the morphological characters. Cytocompatibility studies and tissue regeneration properties were assessed on Saos-2 cells.Results: TEM photograph of TONFC showed fibrous nanostructure. The selected formulation “Ca-IHS4” composed of TONFC+15% P407+10% TCP showed the most prolonged release pattern for 12 days with the least burst effect (about 25% within 24 h). SEM micro-photographs of the in-situ formed scaffolds showed a highly porous 3D structure. Cytocompatibility studies of formulation “Ca-IHS4” revealed the biocompatibility as well as improved cell adhesion, alkaline phosphatase enzyme activity and calcium ion deposition.Conclusion: The outcomes suggest that Ca-IHS4 presents a simple, safe-line and non-invasive strategy for bone regeneration.Keywords: nanofibrillated cellulose, raloxifene hydrochloride, calcium phosphate, in-situ forming hydrogel scaffolds, bone regeneration

Abstract\nHIGHLIGHTSA Newtonian nanofluid containing suspended nanoparticles can substantially improve heat transfer due to enhanced energy transport mechanisms. This theoretical study investigates heat and mass transfer in biological tissues using such a nanofluid under a magnetic field. These properties have promising medical and engineering applications. The nonlinear governing equations were transformed into ordinary differential equations using similarity variables and numerically solved with MATLAB boundary value problem solver bvp4c, subject to appropriate boundary conditions. Results demonstrated increasing the heat source parameter dramatically raised tumor interstitial temperature. This heating, along with improved nanoparticle accumulation within the tumor due to the thermal effects, are together essential for effective hyperthermia treatment. The model provides new insights into tuning heat and mass transport mechanisms in biological tissues via nanofluids for therapeutic applications. Therefore, the findings of this study may improve the efficacy of thermal therapy in treating cancer.This work examined magnetic field effects on heat transfer and nanoparticle (NP) transport in a Newtonian nanofluid within tissue surrounding a blood vessel.Elevating the external heat source power distributes NPs and increases tumor temperature.Boosting the thermophoresis coefficient enhances NP dispersion into tissue.Tuning heat and mass transport mechanisms via nanofluids shows promise for advancing hyperthermia cancer treatment.This work examined magnetic field effects on heat transfer and nanoparticle (NP) transport in a Newtonian nanofluid within tissue surrounding a blood vessel.Elevating the external heat source power distributes NPs and increases tumor temperature.Boosting the thermophoresis coefficient enhances NP dispersion into tissue.Tuning heat and mass transport mechanisms via nanofluids shows promise for advancing hyperthermia cancer treatment. [ABSTRACT FROM AUTHOR]

To obtain a healthy human being with beneficial microflora against different pathogenic infections, classical antibiotics with nanosized biomaterials were used to inhibit the growth of bacterium by their potent synergistic effect. Hence, this study planned to load an oxazolidinone antibiotic named linezolid (LD) onto functionalized chitosan (CN) with 3, 5- dinitrosalyslic acid (DA) via microwave synthesis without harsh condition. The exploring synergistic effect of linezolid (LD) with CN/DA controllable nanostructure was compact efflux-mediated methicillin-resistant Staphylococcus aureus (MRSA) burden and other selected bactericide Gram-positive ((S. aureus), Gram-negative (E. coli), Fungi (C. albicans), Yeast (A. niger), and E. faecalis. The obtained results showed that LD was incorporated into both the internal and external surface of the aggregated CN/DA nanosystem with an average diameter of 150 nm ± 4 hints of the drug loading. Owing to the nature of functionalized CN, the release efficiency attains 98.4% within 100 min. The designed LD@CN/DA exhibited inhibition zone 54 mm, 59 mm, 69 mm, 54 mm, 57 mm, and 24 mm against the tested microbes respectively rather than individual LD. The major target of the current research is achieved by using LD@CN/DA as a nanoantibiotic system that has exceptional consistently active against multi-resistant pathogens, in between MRSA which resist LD. Also, cell viability was performed even after three days of direct cell culture on the surface of the designed nanoantibiotic. The mechanism of microbial inhibition was correlated and rationalized to different charges and the presence of oxygen species against microbial infections. Our findings provide a deep explanation about nanostructured antibiotics design with enhanced potentially pathogen-specific activity.