In drug delivery, enzyme-responsive drug carriers are becoming increasingly relevant because of the growing association of disease pathology with enzyme overexpression. Polymersomes are of interest to such applications because of their tunable properties. While polymersomes open up a wide range of chemical and physical properties to explore, they also present a challenge in developing generalized rules for the synthesis of novel systems. Motivated by this issue, in this perspective, we summarize the existing knowledge on enzyme-responsive polymersomes and outline the main design choices. Then, we propose heuristics to guide the design of novel systems. Finally, we discuss the potential of an integrated approach using computer simulations and experimental studies to streamline this design process and close the existing knowledge gaps.
In this present study, Karpura shilajit bhasma, an Ayurvedic herbo-mineral formulation, currently used in the Ayurvedic clinical practice as a diuretic drug, was investigated chemically and pharmacologically. Content of iron and nitrogen were determined by volumetric analysis and content of calcium, magnesium and aluminium by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES). LD 50 , gross behavioral studies and diuretic activity were evaluated in experimental animals.Calcium was found to be the major element (24.6044% w/w). The LD 50 was found to be 4.625 g/kg p.o. body weight in mice. Karpura shilajit bhasma produced mild reduction in motor coordination and mild sedation during the first 2 h after administration at the doses of 500-5000 mg/kg p.o. in mice. The diuretic activity was found to be significant (P < 0.01) at minimum dose of 200 mg/kg p.o. in rats and dose dependant up to 1000 mg/kg p.o. Furthermore, natriuretic effect was found to be significant (P < 0.01), while no significant change was observed on urinary potassium excretion. The present study justified the use of Karpura shilajit bhasma as a diuretic drug. The results of this study could be used as a model data in the standardization of Karpura shilajit bhasma.
A case of pseudomonas aeruginosa meningitis secondary to chronic otitis media was successfully treated with ceftazidime and gentamicin intravenously. No intrathecal antibiotics were necessary. Treatment of pseudomonas meningitis has been simplified with the advent of third generation cephalosporins.
Angiogenesis represents an excellent therapeutic target for the treatment of cardiovascular diseases. It is a potent physiological process that underlies the natural manner in which our bodies respond to a diminution of blood supply to vital organs, namely the production of new collateral vessels to overcome the ischemic state. This present study is aimed to evaluate and quantify the Angiogenic potential of Terminalia bellirica Roxb, by in vivo mice sponge implantation assay. Here, gelatin sponge with or without Ethanolic extract of Terminalia bellirica leaf (EETB - 0.3 mg and 0.5 mg, respectively) were subcutaneously injected into Swiss albino mice, and 14 days later, the implanted sponges was excised and histologically examined. The stained section showed that sponge containing EETB had produced more vessels in gels than sponges alone. The new vessels were abundantly filled with intact Red blood corpuscles (RBCs), which indicate the formation of a functional vasculature inside the sponges and blood circulation in newly formed vessels by angiogenesis which is induced by EETB. It also measured that the hemoglobin content inside the sponges: Whereas, hemoglobin in control was nearly 0.3 μg, EETB cases the hemoglobin quantity was markedly enhanced to about 17 μg. Taken together, it demonstrated that Ethanolic extract of Terminalia bellirica leaf exhibited a profound angiogenic activity in vivo. The phytochemical screening and qualitative instrumental analysis of EETB reveals the presence of proteins and Phytosterols. The promising angiogenic potential may be due to the presence of the above chemical constituents. Further study is required to define more precisely the molecular mechanisms by which Ethanolic extract of Terminalia bellirica leaf modulates endothelial cell function and gene expression, as well as the pathological relevance of these findings.
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