Enhancement of Aqueous Solubility, Dissolution Profile, and Oral Bioavailability of Pentoxifylline by Microsponges

A. Pawar, N. A. Shete, P. Jadhav, V. Deshmukh, J. Mehetre
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引用次数: 1

Abstract

Microsponge, a novel drug delivery system, is designed to deliver a pharmaceutically active ingredient efficiently at the minimum dose. Microsponge plays an important role in enhancing drug stability, reducing side effects, and modifying drug release profiles. It is mostly used for transdermal delivery. Recent studies also explored their use for oral administration. This study aimed to explore the potential use of the microsponge technique in improving the aqueous solubility and dissolution profile of pentoxifylline (PTX). In this study, microsponges were prepared by a quasi-emulsion solvent diffusion method by varying concentrations of carriers. Nine different ratios of the PTX:Eudragit E-100 with varying amounts of dichloromethane were used. All formulated microsponges were evaluated for %production yield, compatibility of drug excipient, encapsulation efficiency, in vitro drug release, and in vivo bioavailability, as well as recorded by scanning electron microscopy (SEM) and differential scanning calorimetry(DSC). Our data suggested that the aqueous solubility of PTX microsponges was four times greater than that of pure drug. The in vitro drug release of selected microsponges (M8) was found to be 70%; furthermore, the in vivo study suggested that the selected formulation significantly enhanced drug concentration in the plasma (9,219 ng/mL in 12 hours) in comparison to pure drug PTX (2,476 ng/mL in 12 hours). SEM showed that the prepared microsponges were spherical with porous nature. Fourier-transform infrared spectroscopy and DSC studies confirmed an absence of incompatibility among drugs and selected excipients. The pH of the selected gel was found to be 6.8, which was compatible with those of skin and oral formulations also. All above data suggested a highly successful and beneficial use of the microsponge technique in enhancing aqueous solubility, dissolution profile, and oral bioavailability of PTX. Microsponge-based delivery of PTX may represent an alternative strategy to improve the bioavailability of the drug.
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微海绵增强己酮可可碱的水溶性、溶出度和口服生物利用度
Microsponge是一种新型的给药系统,其设计目的是以最小剂量有效地递送药物活性成分。微海绵在提高药物稳定性、减少副作用、改变药物释放谱等方面发挥着重要作用。它主要用于经皮给药。最近的研究也探讨了它们用于口服给药。本研究旨在探讨微海绵技术在改善己酮茶碱(PTX)水溶性和溶解谱方面的潜在应用。本研究采用准乳状溶剂扩散法,通过不同浓度的载体制备微海绵。使用了九种不同比例的PTX:Eudragit E-100和不同数量的二氯甲烷。采用扫描电镜(SEM)和差示扫描量热法(DSC)对配制的微海绵进行了产率、药物赋形剂相容性、包封效率、体外药物释放度和体内生物利用度的评价。我们的数据表明,PTX微海绵的水溶性是纯药物的4倍。所选微海绵(M8)的体外释药率为70%;此外,体内研究表明,与纯药物PTX (2476 ng/mL, 12小时)相比,所选制剂显著提高了血浆中药物浓度(12小时9,219 ng/mL)。SEM结果表明,制备的微海绵呈球形,具有多孔性。傅里叶变换红外光谱和DSC研究证实药物和所选辅料之间不存在不相容性。所选凝胶的pH值为6.8,与皮肤和口服制剂的pH值基本一致。以上数据表明,微海绵技术在提高PTX的水溶性、溶出度和口服生物利用度方面是非常成功和有益的。以微海绵为基础的PTX递送可能是提高药物生物利用度的另一种策略。
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