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帕利哌酮基于环糊精的 pH 响应原位鼻腔凝胶的研制与评价。

Development and Evaluation of pH-Responsive Cyclodextrin-Based in situ Gel of Paliperidone for Intranasal Delivery.

机构信息

Department of Pharmaceutical Chemistry & Quality Assurance, SVKM's Dr. Bhanuben Nanavati College of Pharmacy, Vile Parle (W), Mumbai, 400056, India.

Department of Pharmaceutics, SPP School of Pharmacy & Technology Management, SVKM's NMIMS, Vile Parle (W), Mumbai, 400056, India.

出版信息

AAPS PharmSciTech. 2018 Jan;19(1):384-394. doi: 10.1208/s12249-017-0844-8. Epub 2017 Jul 26.

Abstract

Paliperidone (PLPD) is approved for treatment and management of schizophrenia. The current study demonstrates the potential of in situ gel of PLPD for nasal delivery. The permeation of drug through sheep nasal mucosa was analyzed since the nose-to-brain pathway has been indicated for delivering drugs to the brain. The carbopol 934 (CP)- and hydroxypropyl methyl cellulose K4M (HPMC)-based in situ gels containing 0.2% CP and 0.4% w/v HPMC were optimized using experimental design software. The use of hydroxypropyl-β-cyclodextrin (HP-β-CD) in nasal permeation of drug was investigated. Transmucosal permeation of PLPD was examined using sheep nasal mucosa. The in situ gels of PLPD exhibited satisfactory mucoadhesion and showed sustained drug release. The mucocilliary toxicity and histopathological examination confirmed that the nasal mucosa architecture remains unaffected after treatment with PLPD in situ gel. The formulation containing HP-β-CD complex of PLPD exhibited higher rate of drug permeation through sheep nasal mucosa revealing the role of HP-β-CD as nasal absorption enhancer. Thus, CP- and HPMC-based pH-triggered in situ gel containing HP-β-CD-drug inclusion complex demonstrates a novel nasal delivery of PLPD.

摘要

帕利哌酮(PLPD)被批准用于治疗和管理精神分裂症。本研究旨在展示 PLPD 原位凝胶作为鼻腔给药的潜力。由于鼻内给药可将药物递送至大脑,因此分析了药物通过绵羊鼻黏膜的渗透情况。使用实验设计软件对含有 0.2% CP 和 0.4% w/v HPMC 的 CP-和羟丙基甲基纤维素 K4M(HPMC)为基础的原位凝胶进行了优化。考察了羟丙基-β-环糊精(HP-β-CD)在药物鼻腔渗透中的作用。使用绵羊鼻黏膜检查 PLPD 的经黏膜渗透情况。PLPD 的原位凝胶具有令人满意的黏膜黏附性,并表现出持续的药物释放。黏膜纤毛毒性和组织病理学检查证实,用 PLPD 原位凝胶处理后,鼻黏膜结构不受影响。含有 PLPD-HP-β-CD 包合物的制剂表现出更高的药物透过绵羊鼻黏膜的速率,表明 HP-β-CD 作为鼻内吸收增强剂的作用。因此,CP 和 HPMC 为基础的 pH 触发原位凝胶,含有 HP-β-CD-药物包合物,展示了一种新型的 PLPD 鼻腔给药方式。

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