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电泳(离子电渗法)增强了高分子聚合物从口腔黏膜中的传递。

Delivery of macromolecules across oral mucosa from polymeric hydrogels is enhanced by electrophoresis (iontophoresis).

机构信息

Oral Growth and Development, Dental Physical Sciences, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, London, United Kingdom.

出版信息

Dent Mater. 2013 Nov;29(11):e299-307. doi: 10.1016/j.dental.2013.09.003. Epub 2013 Sep 30.

Abstract

OBJECTIVE

To develop polymeric hydrogel delivery systems for iontophorseis transfer of large molecules across buccal (porcine) mucosa.

METHODS

Three hydrogels (PVA, HPMC and PVA/HPMC) were prepared as stable gels (7 mm diameter/1.5 mm thick). Quantitative (8 and 36 h) assessment of porcine buccal mucosa and the three hydrogel delivery systems, using a diffusion cell in vitro model, was carried out by UV/vis spectroscopy with three model agents (3 and 10 kDa dextrans and 12 kDa parvalbumin). Passive and iontophoresis parameters were obtained. Experimental and theoretical data were compared.

RESULTS

Iontophoresis (30 min, 1-8 h) significantly enhanced the delivery of all model agents across four single systems (hydrogels and buccal mucosa) and three sandwich systems (hydrogels on top of buccal mucosa), as confirmed by time lag factor/enhancement ratio (TLF/ER) data. The diffusion coefficients of model agents across buccal mucosa (×10(-13) m(2) s(-1)) were ~100 times lower than across single hydrogels (2.97-4.80×10(-11) m(2) s(-1)). Solubility values of all agents across hydrogels were similar, but lower across buccal mucosa. Permeability of parvalbumin was highest across PVA, and for both dextrans across PVA/HPMC. In sandwich systems TLFs were similar for all hydrogels, but significantly lower, and ERs significantly higher, than tissue alone. Experimental and theoretical TLF data were in reasonable agreement.

SIGNIFICANCE

The in vitro data show that iontophoresis enhanced the delivery of large molecules across polymeric hydrogel systems and buccal mucosa. This creates the opportunity of new approaches to drug delivery and opens pathways to further research for delivering therapeutic agents topically and systemically.

摘要

目的

开发聚合物水凝胶递药系统,以实现大分子经颊(猪)黏膜的电渗透传递。

方法

制备三种水凝胶(PVA、HPMC 和 PVA/HPMC)作为稳定凝胶(7mm 直径/1.5mm 厚)。采用体外扩散池模型,通过紫外/可见分光光度法,使用三种模型药物(3 和 10kDa 葡聚糖和 12kDa 副肌球蛋白)对猪颊黏膜和三种水凝胶递药系统进行定量(8 和 36h)评估。获得被动和电渗透参数。比较实验和理论数据。

结果

电渗透(30min,1-8h)显著提高了所有模型药物在四个单一系统(水凝胶和颊黏膜)和三个三明治系统(水凝胶置于颊黏膜之上)中的传递,这一点通过时滞因子/增强比(TLF/ER)数据得到证实。模型药物经颊黏膜(×10(-13)m(2)s(-1))的扩散系数比单一水凝胶(2.97-4.80×10(-11)m(2)s(-1))低约 100 倍。所有药物在水凝胶中的溶解度值相似,但在颊黏膜中较低。副肌球蛋白在 PVA 中的渗透性最高,两种葡聚糖在 PVA/HPMC 中均较高。在三明治系统中,所有水凝胶的 TLF 相似,但显著低于单独组织的 TLF,ER 则显著高于单独组织的 ER。实验和理论 TLF 数据具有较好的一致性。

意义

体外数据表明,电渗透增强了大分子经聚合物水凝胶系统和颊黏膜的传递。这为药物传递提供了新的方法,并为局部和系统递药以治疗疾病开辟了新的研究途径。

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