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用于眼科药物递送的原位形成凝胶。

In situ-forming gels for ophthalmic drug delivery.

作者信息

Kumar S, Haglund B O, Himmelstein K J

机构信息

Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha.

出版信息

J Ocul Pharmacol. 1994 Spring;10(1):47-56. doi: 10.1089/jop.1994.10.47.

Abstract

Poor bioavailability of ophthalmic solutions caused by dilution and drainage from the eye can be overcome by using in situ-forming ophthalmic drug delivery systems prepared from polymers that exhibit reversible phase transitions. Joshi et al. (1), have demonstrated that aqueous compositions that reversibly gel in response to simultaneous variations in at least two physical parameters, such as temperature, pH, and ionic strength, can be formed by appropriate combinations of macromolecular polymers which exhibit reversible gelation properties. In the present study, the rheological characterization of such a system, prepared by a combination of Carbopol (C) and methyl cellulose (MC), was carried out at two different pH (4.0 and 7.4) and temperatures (25 and 37 degrees C) by rotational cone and plate viscometry. The shear stress (tau) vs. shear rate (D) flow curves of the aqueous polymer solutions indicated a pseudoplastic behavior, with a yield point. An increase in pH from 4.0 to 7.4, or temperature from 25 to 37 degrees C, resulted in an increase in viscosity (eta), tau, and yield point, the magnitude of changes being highest when both the parameters were altered simultaneously. An increase in concentration of either C or MC, or an increase in MC molecular weight results in an increase in eta, tau, and yield point. Among the compositions studied, a solution containing 1.5% MC 0.3% C was found to have low eta, and formed a strong gel under simulated physiological conditions. Such a system can be formulated as drug containing liquid suitable for administration by instillation into the eye, which upon exposure to physiological conditions will shift to the gel (semi-solid) phase, thus increasing the precorneal residence time of the delivery system and enhancing ocular bioavailability.

摘要

眼部溶液因眼部稀释和排出导致的生物利用度差问题,可以通过使用由具有可逆相变的聚合物制备的原位形成眼部给药系统来克服。乔希等人(1)已经证明,通过具有可逆凝胶化特性的大分子聚合物的适当组合,可以形成响应至少两个物理参数(如温度、pH值和离子强度)同时变化而可逆凝胶化的水性组合物。在本研究中,通过旋转锥板粘度法在两种不同的pH值(4.0和7.4)和温度(25和37摄氏度)下,对由卡波姆(C)和甲基纤维素(MC)组合制备的此类系统进行了流变学表征。聚合物水溶液的剪切应力(τ)与剪切速率(D)的流动曲线显示出假塑性行为,并具有屈服点。pH值从4.0增加到7.4,或温度从25摄氏度增加到37摄氏度,都会导致粘度(η)、τ和屈服点增加,当两个参数同时改变时,变化幅度最大。C或MC浓度的增加,或MC分子量的增加,都会导致η、τ和屈服点增加。在所研究的组合物中,发现含有1.5%MC和0.3%C的溶液具有低η,并在模拟生理条件下形成强凝胶。这样的系统可以配制成适合通过滴眼给药的含药液体,其在暴露于生理条件时将转变为凝胶(半固体)相,从而增加给药系统在角膜前的停留时间并提高眼部生物利用度。

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