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首页> 外文期刊>Drug delivery and translational research >Chlorpheniramine maleate containing chitosan-based nanoparticle-loaded thermosensitive in situ gel for management in allergic rhinitis
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Chlorpheniramine maleate containing chitosan-based nanoparticle-loaded thermosensitive in situ gel for management in allergic rhinitis

机译:含氯苯胺马来酸含壳聚糖的纳米粒子纳米粒子载热敏,用于过敏性鼻炎的管理

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摘要

The aim of the present study was to fabricate a thermosensitive gel containing chlorpheniramine maleate (CPM)-loaded nanoparticles following intranasal administration for effective treatment of allergic rhinitis. Chitosan-based nanoparticles were prepared by a precipitation method followed by the addition of developed NPs within the poloxamer 407- and carbopol 934P-based mucoadhesive thermoreversible gel. Developed formulations were evaluated for particle size, PDI, % entrapment efficiency, and % cumulative drug permeation. NP3 formulation was found to be optimized on the basis of minimum particle size (143.9 nm), maximum entrapment efficiency (80.10 +/- 0.414%), and highest drug permeation (90.92 +/- 0.531%). The optimized formulation NP3 was then formulated into thermoreversible in situ gel. This intensifies the contact between the nasal mucosa and the drug and increases and facilitates the drug absorption which results in increased bioavailability. G4 formulation was selected as the optimized formulation on the basis of gelation ability and mucoadhesive strength. Histology was carried out to examine the damage caused by the optimized G4 formulation. Results revealed no visual signs of tissue damage thus indicated safe nasal delivery of nanoparticulate in situ gel formulation G4. Thus, intranasal CPM NP-loaded in situ gel was found to be a promising formulation for the management of allergic rhinitis.
机译:本研究的目的是制造含有含氯苯胺的热敏凝胶,其在鼻内给药后含有氯苯胺(CPM)加载的纳米颗粒,以有效治疗过敏性鼻炎。通过沉淀方法制备基于壳聚糖的纳米颗粒,然后在泊洛沙姆407-和Carbopol 934p的粘膜粘附热可逆凝胶中添加发育的NP。评估研制的制剂用于粒度,PDI,%夹带效率和累积药物渗透的%。发现NP3配方在最小粒径(143.9nm)的基础上进行优化,最大夹带效率(80.10 +/- 0.414%)和最高药物渗透(90.92 +/- 0.531%)。然后将优化的制剂NP3配制成热可逆的原位凝胶。这加剧了鼻腔粘膜和药物之间的接触,并增加并促进药物吸收,这导致增加生物利用度。基于凝胶化能力和粘膜粘附强度选择G4制剂作为优化的制剂。进行组织学,以检查由优化的G4配方引起的损伤。结果表明,由于原位凝胶制剂G4,因此没有表明纳米颗粒的安全性鼻腔递送的可视迹象。因此,发现Intranasal CPM in in原位凝胶负载是对过敏性鼻炎的管理的有希望的制剂。

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