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Ca2+ Efflux from Temperature Sensitive Liposomes and In Situ Formation of Metal Cholate Liposome Gels: Basic Studies and Potentials for Sustained Site-Specific Drug Delivery

机译:来自温度敏感脂质体的Ca 2+外排和金属胆酸盐脂质体凝胶的原位形成:基础研究和持续特定部位给药的潜力

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Liposomes or vesicles are biomimetic close containers for the delivery of drugs at the local site for an extended period of time. On the other hand hydrogels which are three-dimensional hydrophilic matrices are another class of popular materials for sustained release. Such hybrids combine the features of liposomes and polymer to ensure a sustained local drug delivery. In the present work a novel liposome/hydrogel soft assembly is explored which may be potentially useful for drug delivery applications. We report thermally triggered release of Ca +2 from temperature sensitive liposomal compartments constituted as 90 mol% DPPC and 10 mol% DMPC to induce rapid gelation of a solution of calcium cholate and AgNO 3 (extravesicular precursor fluid). Calcium chloride loaded liposomes were prepared using the lipid film rehydration method. The formation of unilamellar bilayer were supported by the fluorometric studies using a compatible and labeled fluoropore (NBD-PS). Hydrogels were obtained by mixing Ca +2 loaded liposome with extravesicular precursor fluid and incubating the content at 37 o C. The concentration of the cholate during gelation was sublytic in order to avoid vesicle solubilization. The integrity of liposomes within the hydrogels were preserved during gelation as confirmed by transmission electron microscopy (TEM). The presence of low concentration of cholate (for example 0.05 mM) also permitted spectrophotometric monitoring of Ca +2 efflux for Ca-vesicles employing calcium sensitive dye, Arsenazo III. We expect that this simple experiment may also be useful for developing implantable as well as rapidly gelling injectable biomaterials for site-specific drug delivery. The present work is also significant as the antimicrobial properties of hydrogels containing silver has been widely recognized for its therapeutic profile.
机译:脂质体或囊泡是仿生的密闭容器,用于在本地站点较长时间内输送药物。另一方面,作为三维亲水性基质的水凝胶是另一类持续释放的流行材料。这样的杂合体结合了脂质体和聚合物的特征,以确保持续的局部药物递送。在本工作中,探索了新颖的脂质体/水凝胶软组装,其对于药物递送应用可能潜在地有用。我们报道了热触发的Ca + 2从构成90 mol%DPPC和10 mol%DMPC的温度敏感性脂质体区室释放,以诱导胆酸钙和AgNO 3(囊外前体液)溶液快速凝胶化。使用脂质膜再水化方法制备了装载氯化钙的脂质体。单层双层的形成通过使用相容且标记的氟孔(NBD-PS)的荧光分析研究得到支持。通过将负载Ca +2的脂质体与囊外前体液混合并在37°C下温育内容物来获得水凝胶。凝胶化过程中胆酸盐的浓度被分解,以避免囊泡增溶。如通过透射电子显微镜(TEM)所证实的,在凝胶化过程中保留了水凝胶内脂质体的完整性。低浓度胆酸盐(例如0.05 mM)的存在还允许使用钙敏感染料Arsenazo III对钙小泡的Ca +2外排进行分光光度法监测。我们希望这个简单的实验对于开发可植入的以及快速胶凝的可注射生物材料用于定点药物递送也可能有用。由于含银水凝胶的治疗特性已被广泛认可,因此本研究也具有重要意义。

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