Russo Jackson, Fiegel Jennifer, Brogden Nicole K
Department of Pharmaceutical Sciences and Experimental Therapeutics, The University of Iowa, Iowa City, IA 52242, USA.
Department of Chemical and Biochemical Engineering, The University of Iowa, Iowa City, IA 52242, USA.
Pharmaceutics. 2020 Dec 15;12(12):1214. doi: 10.3390/pharmaceutics12121214.
Chronic wounds are a significant and growing health problem, and clinical treatment is often a painful experience. A topical dosage form would be optimal to treat this pain. Poloxamer 407, a thermosensitive polymer that is a liquid at low temperatures but gels at higher temperatures, is well suited to administer topical analgesics to chronic wound sites. The goal of this study was to evaluate the gelation and drug delivery properties of poloxamer 407 gels containing diclofenac sodium for potential use in chronic wound analgesic delivery. The gelation properties of poloxamer formulations were evaluated rheologically. Drug delivery properties of poloxamers loaded with diclofenac sodium were evaluated using snakeskin dialysis membranes, intact porcine ear skin, and porcine ear skin impaired via tape stripping. A commercial gel product and a solution of diclofenac sodium in water were used as control formulations. Poloxamer concentration and gelation temperature varied inversely, and the addition of higher concentrations of diclofenac sodium correlated to significant increases in poloxamer gelation temperature. Poloxamer solutions were effective in limiting the permeation of diclofenac sodium through membranes with impaired barrier properties, and delivery of diclofenac sodium from poloxamer 407 did not vary significantly from delivery observed from the commercial gel product. The amount of drug delivered in 24 h did not change significantly with changes in poloxamer 407 concentration. The results of this study indicate that poloxamer 407 may be a useful formulation component for administration of an analgesic product to a chronic wound site.
慢性伤口是一个日益严重的重大健康问题,临床治疗往往是一种痛苦的经历。局部剂型对于治疗这种疼痛将是最佳选择。泊洛沙姆407是一种热敏聚合物,在低温下为液体,但在较高温度下会形成凝胶,非常适合于向慢性伤口部位局部给药镇痛药。本研究的目的是评估含有双氯芬酸钠的泊洛沙姆407凝胶的凝胶化和药物递送特性,以用于慢性伤口镇痛递送的潜在用途。通过流变学评估泊洛沙姆制剂的凝胶化特性。使用蛇皮透析膜、完整的猪耳皮肤和通过胶带剥离受损的猪耳皮肤评估负载双氯芬酸钠的泊洛沙姆的药物递送特性。一种市售凝胶产品和双氯芬酸钠水溶液用作对照制剂。泊洛沙姆浓度与凝胶化温度呈反比,较高浓度双氯芬酸钠的添加与泊洛沙姆凝胶化温度的显著升高相关。泊洛沙姆溶液可有效限制双氯芬酸钠透过屏障性能受损的膜的渗透,并且双氯芬酸钠从泊洛沙姆407中的递送与从市售凝胶产品中观察到的递送没有显著差异。24小时内递送的药物量不会随泊洛沙姆407浓度的变化而显著改变。本研究结果表明,泊洛沙姆407可能是一种用于向慢性伤口部位给药镇痛产品的有用制剂成分。