Recent Advances In The Development Of Nanoparticles In Enhancement Of Solubility Of Poorly Soluble Drugs

Q3 Pharmacology, Toxicology and Pharmaceutics
Pavan Kumar Krosuri , Mothilal M
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Abstract

The formulation of poorly soluble drugs is one of the most difficult tasks for pharmaceutical formulators. Conventional techniques for increasing the solubility of these drugs have had limited success. This is especially true when dealing with drugs that have low aqueous and organic solubility. Solubility is an important determinant of drug liberation and thus drug absorption, and it plays an important role in formulation oral bioavailability. A drug solubility directly influences its dissolution rate. Most New drugs have low water solubility, making them difficult to formulate into drug delivery systems. As a result, improving the solubility of poorly water soluble drugs is one of the necessary preformulation steps in pharmaceutical product development research. The use of nanoparticles in the formulation of hydrophobic drugs improves their solubility and efficacy. Emulsion-solvent evaporation method, Double Emulsion and Evaporation method, Salting out method, Emulsions diffusion method, Antisolvent Precipitation Method, Polymerization method, and Coacervation or Ionic Gelation method can all be used to make nanoparticles. Bottom-up methods such as Antisolvent precipitation are the most efficient and cost effective in the preparation of nanoparticles.
纳米颗粒增强难溶性药物溶解度的研究进展
配制难溶性药物是制剂师最困难的任务之一。提高这些药物溶解度的传统技术取得了有限的成功。在处理水溶性和有机溶解度较低的药物时尤其如此。溶解度是药物释放和吸收的重要决定因素,在制剂的口服生物利用度中起着重要作用。药物的溶解度直接影响其溶出速率。大多数新药的水溶性较低,这使得它们难以配制成药物输送系统。因此,提高难水溶性药物的溶解度是药品开发研究中必要的预处方步骤之一。在疏水药物的配方中使用纳米颗粒可以提高其溶解度和疗效。乳液-溶剂蒸发法、双乳液和蒸发法、盐析法、乳液扩散法、反溶剂沉淀法、聚合法、凝聚或离子凝胶法都可以用来制备纳米颗粒。反溶剂沉淀法等自下而上的方法是制备纳米粒子最有效和最经济的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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