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将硝苯地平载入原位眼用凝胶进行再利用,作为治疗青光眼的新方法。

Repurposing of nifedipine loaded in situ ophthalmic gel as a novel approach for glaucoma treatment.

机构信息

Department of Pharmaceutics, Faculty of Pharmacy, Modern University for Technology and Information (MTI), Cairo, Egypt.

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, Egypt.

出版信息

Biomed Pharmacother. 2021 Oct;142:112008. doi: 10.1016/j.biopha.2021.112008. Epub 2021 Aug 9.

Abstract

Glaucoma is a chronic eye disease characterized by elevated intraocular pressure (IOP) which causes severe complications to the eyes and may lead to vision loss. The effective treatment of such diseases motivated the search for novel and unique drugs and delivery systems. It has been reported that, nifedipine (NF) is effective in reducing the elevated IOP due to vasodilatation of eye vascular smooth muscles. NF loaded thermo-sensitive in situ gels were prepared by the cold method using poloxamer 407 (P407) and hydroxypropyl methyl cellulose (HPMC) polymers adopting Box-Behnken experimental design. All the prepared formulae were tested for homogeneity, clarity, pH, isotonicity, gelling capacity, rheological behavior, in vitro drug release and were tested in vivo on rabbits. The prepared in situ gels were homogenous, transparent, having a pH ranged from 5 to 5.5 and undergo sol-gel transition within few seconds physiological temperature. The in situ gels showed sustained in vitro release of NF where about 76% of the loaded drug was released over 12 h. NF loaded in situ gels showed a 45.83 ± 2.91% reduction in the IOP, with no sign of toxicity or irritation to the eye in rabbits. The current investigations clarified the efficiency of this novel and unique NF loaded in situ gel for the control of the IOP compared to the conventional ophthalmic dosage forms.

摘要

青光眼是一种慢性眼病,其特征是眼内压(IOP)升高,会对眼睛造成严重的并发症,并可能导致视力丧失。为了有效治疗此类疾病,人们一直在寻找新型独特的药物和给药系统。有报道称,硝苯地平(NF)通过扩张眼部血管平滑肌,可有效降低升高的 IOP。采用 Box-Behnken 实验设计,使用泊洛沙姆 407(P407)和羟丙基甲基纤维素(HPMC)聚合物,通过冷法制备 NF 载热敏原位凝胶。对所有制备的配方进行均匀性、澄清度、pH 值、等渗性、胶凝能力、流变行为、体外药物释放以及在兔子体内进行测试。所制备的原位凝胶均匀透明,pH 值在 5 到 5.5 之间,在几秒钟的生理温度下发生溶胶-凝胶转变。原位凝胶表现出 NF 的持续体外释放,约 76%的载药在 12 小时内释放。NF 载原位凝胶可使 IOP 降低 45.83±2.91%,对兔子的眼睛没有毒性或刺激性。目前的研究结果表明,与传统的眼部剂型相比,这种新型独特的 NF 载原位凝胶在控制 IOP 方面具有更好的效果。

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