首页> 外文OA文献 >Supercritical solvent impregnation of poly(ɛ-caprolactone)/poly(oxyethylene-b-oxypropylene-b-oxyethylene) and poly(ɛ-caprolactone)/poly(ethylene-vinyl acetate) blends for controlled release applications
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Supercritical solvent impregnation of poly(ɛ-caprolactone)/poly(oxyethylene-b-oxypropylene-b-oxyethylene) and poly(ɛ-caprolactone)/poly(ethylene-vinyl acetate) blends for controlled release applications

机译:聚(ε-己内酯)/聚(氧乙烯-b-氧丙烯-b-氧乙烯)和聚(ε-己内酯)/聚(乙烯-醋酸乙烯酯)混合物的超临界溶剂浸渍

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摘要

Poly(ɛ-caprolactone) blends were successfully impregnated with timolol maleate, an anti-glaucoma drug, using a supercritical solvent impregnation (SSI) technique. Supercritical fluid impregnation efficiency results suggested that the best impregnating conditions were obtained when a cosolvent was used and when specific drug–polymer interactions occurred as a consequence of different chemical structures due to polymer blending. Pressure can be either a favourable factor, when there is enough drug affinity for the polymers, or an unfavourable factor when weaker bonding is involved. In order to determine the relative hydrophilicity/hydrophobicity of the blends, contact angle analysis was performed, while crystallinity determination was also useful to understand the obtained release profiles.Drug loading, heterogeneous/homogeneous dispersion of drug inside the matrix, hydrophilicity, crystallinity, all seem to influence the obtained drug release rates. The “in vitro” release results suggested that a sustained drug release rate can be obtained by changing the SSI operational conditions and by modulating the composition of blends, as a mean to control crystallinity, hydrophilicity and drug affinity for the polymer matrix. After a first day burst release, all samples showed a sustained release profile (1.2–4 μg/(ml day), corresponding to a mass of 3–10 μg/day) which is between the therapeutic and toxic levels of timolol maleate, during a period of 1 month. These drug-loaded polymeric matrices can be a feasible alternative treatment modality for the conventional repeated daily administration of eye drops.
机译:使用超临界溶剂浸渍(SSI)技术成功地将抗青光眼药物马来酸替莫洛尔浸渍了聚(ε-己内酯)混合物。超临界流体浸渍效率结果表明,当使用助溶剂以及由于聚合物共混而导致的不同化学结构导致特定的药物-聚合物相互作用时,可获得最佳的浸渍条件。当对聚合物有足够的药物亲和力时,压力可能是一个有利因素,而当涉及较弱的键合时,压力可能是不利因素。为了确定共混物的相对亲水性/疏水性,进行了接触角分析,而结晶度的确定也有助于理解所获得的释放曲线。药物载量,基质内药物的异质/均匀分散,亲水性,结晶度,所有似乎影响获得的药物释放速率。 “体外”释放结果表明,可以通过改变SSI操作条件和调节共混物的组成来获得持续的药物释放速率,以此作为控制聚合物基质的结晶度,亲水性和药物亲和力的手段。爆裂释放的第一天后,所有样品在治疗期间和毒性毒性水平之间均表现出持续释放特性(1.2–4μg/(ml天),相当于3–10μg/天的质量)。为期1个月。对于常规的每天重复滴眼液,这些载有药物的聚合物基质可能是可行的替代治疗方式。

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