The methanol extract of the fruit pulp of Adansonia digitata L. (Malvaceae) was examined for its hepatoprotective activity against liver damage induced by acetaminophen in rats. The principle depends on the fact that administration of acetaminophen will be associated with development of oxidative stress. In addition, hepatospecific serum markers will be disturbed. Treatment of the rats with the methanol extract of the fruit pulp of Adansonia digitata L. prior to administration of acetaminophen significantly reduced the disturbance in liver function. Liver functions were measured by assessment of total protein, total bilirubin, ALP, ALT, and AST. Oxidative stress parameter and antioxidant markers were also evaluated. Moreover, histopathological evaluation was performed in order to assess liver case regarding inflammatory infiltration or necrosis. Animals were observed for any symptoms of toxicity after administration of extract of the fruit pulp of Adansonia digitata L. to ensure safety of the fruit extract.

Nanofibers have emerged as advanced fibers with broad use and potential in biomedical fields in recent decades. The process of healing is an innate immune response towards a pathophysiology such as wound. Ordinary time taken for wound healing is approximately 2-3 days depending upon the chronic state. Air moisture and microbes risk pathological manifestations leading to delayed or incomplete palliate process. An external agent that can provide balanced moisture, increasing cell proliferation with microbial infiltration or anti-bacterial activity, aids to speed the healing process. Apart from these qualities, an ideal material should be simple, cost effective, and repeatable. Nanofibers produced through electrospinning have become a promising strategy in the treatment of wounds. Apart from being simple in application, they are produced from natural or synthetic polymers. Nanofibers exhibit high surface area, nanoporosity, with a potential to load potent drugs or enzymes. Other biomedical applications include use of nanofibers as tissue scaffolds and as masking agents in modern cosmetics. Therefore nanofibers are excellent candidates for wound treatment and management. The current review is an attempt to discuss and present literature about different techniques, chemical materials, and entities used to produce efficient electrospun nanofibers for use in pathological, medicinal, or treatment or management of injury or laceration.

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BackgroundInjectable in situ gel (ISG) systems suffer from high initial drug release that may result in toxic effects.ObjectiveThis work aimed to develop an injectable sustained release rosuvastatin (RSV) ISG formulation with minimum initial drug burst and improved hyperlipidemic efficacy.MethodsSix formulation factors that affect RSV release after 0.5, 2 and 24 hrs have been screened and the significant ones were optimized utilizing an experimental design tool. The optimum ISG formulation components were physicochemically characterized. Kinetic treatment, dissolution efficiency and mean dissolution time were investigated for the developed ISG formulations. Pharmacodynamic effects of the optimized ISG formulation were studied and compared to ISG formulation loaded with free RSV and to a marketed oral drug product.ResultsThe concentration polylactide-co-ε-caprolactone (25: 75), the surfactant hydrophilic lipophilic balance (HLB) and the ratio of surfactant to polyethylene glycol 400 were significantly affecting the release of RSV during the first 24 h. Physicochemical characterization demonstrated complete dispersion of RSV in the polymeric matrix with slight changes in the drug crystalline structure. The optimized formulation demonstrated acceptable syringeability, good flow rate and was able to extend the in vitro drug release for 34 days. The ISG formulations complied with Weibull model. Pharmacodynamic study revealed a sustained reduction in the lipid profile that lasted for 21 days with a marked decrease in the lipid level during the first 24 hrs from the ISG system loaded with free RSV.ConclusionThe optimized RSV ISG formulation could be considered a promising strategy due to a reduction in dosing frequency and enhancement in hypolipidemic efficacy.

The antispasmodic drug mebeverine hydrochloride was formulated into a film-forming gel to be used as a topical local anesthetic. A mixture of cellulose derivatives was used as a base. Additives were used to enhance the release as well as the residence time. Formulations were characterized in terms of drug release, mucoadhesion and rheology. Clinically, the selected formula has shown faster onset (p = 0.0156), longer duration (p = 0.0313), better film residence (p = 0.0313), and no foreign body sensation (p = 0.0313) in comparison to Solcoseryl dental paste. Histopathological examination showed no change in inflammatory cells count, concluding that this topical anesthetic is efficacious and safe orally.