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用于含有氢氟烷烃推进剂的压力定量吸入器的反向氟碳包水乳液。

Reverse water-in-fluorocarbon emulsions for use in pressurized metered-dose inhalers containing hydrofluoroalkane propellants.

作者信息

Butz N, Porté C, Courrier H, Krafft M P, Vandamme Th F

机构信息

Laboratoire de Chimie Thérapeutique et Nutritionnelle: Biodisponibilité Tissulaire et Cellulaire, Faculté de Pharmacie, Université Louis Pasteur, 74 Route du Rhin, BP 24, 67401 Illkirch Cedex, France.

出版信息

Int J Pharm. 2002 May 15;238(1-2):257-69. doi: 10.1016/s0378-5173(02)00086-8.

Abstract

Pulmonary administration of drugs has demonstrated numerous advantages in the treatment of pulmonary diseases due to direct targeting to the respiratory tract. It enables avoiding the first pass effect, reduces the amount of drugs administered, targets drugs to specific sites and reduces their side effects. Reverse water-in-fluorocarbon (FC) emulsions are potential drug delivery systems for pulmonary administration using pressurized metered-dose inhalers (pMDI). The external phase of these emulsions consists of perfluorooctyl bromide (PFOB, perflubron), whereas their internal phase contains the drugs solubilized or dispersed in water. These emulsions are stabilized by a perfluoroalkylated dimorpholinophosphate (F8H11DMP), i.e. a fluorinated surfactant. This study demonstrates the possibility of delivering a reverse fluorocarbon emulsion via the pulmonary route using a CFC-free pMDI. Two hydrofluoroalkanes (HFAs) (Solkane(R) 134a and Solkane(R) 227) were used as propellants, and various solution (or emulsion)/propellant ratios (1/3, 1/2, 2/3, 1/1, 3/2, 3/1 v/v) were investigated. The insolubility of water (with or without the fluorinated surfactant F8H11DMP) in both HFA 227 and HFA 134a was demonstrated. PFOB and the reverse emulsion were totally soluble or dispersible in all proportions in both propellants. This study demonstrated also that the reverse FC emulsion can be successfully used to deliver caffeine in a homogeneous and reproducible way. The mean diameter of the emulsion water droplets in the pressured canister was investigated immediately after packaging and after 1 week of storage at room temperature. Best results were obtained with emulsion/propellant ratios comprised between 2/3 and 3/2, and with HFA 227 as propellant.

摘要

由于能直接作用于呼吸道,药物肺部给药在肺部疾病治疗中已显示出诸多优势。它能避免首过效应,减少给药剂量,使药物靶向特定部位并降低副作用。反向氟碳(FC)乳液是使用压力定量吸入器(pMDI)进行肺部给药的潜在药物递送系统。这些乳液的外相由全氟辛基溴(PFOB,全氟溴辛烷)组成,而内相包含溶解或分散于水中的药物。这些乳液由全氟烷基化二吗啉代磷酸酯(F8H11DMP)即一种氟化表面活性剂稳定。本研究证明了使用无氯氟烃的pMDI经肺部途径递送反向氟碳乳液的可能性。使用了两种氢氟烷烃(HFA)(苏尔寿(Solkane®)134a和苏尔寿(Solkane®)227)作为推进剂,并研究了各种溶液(或乳液)/推进剂比例(1/3、1/2、2/3、1/1、3/2、3/1 v/v)。已证明水(含或不含氟化表面活性剂F8H11DMP)在HFA 227和HFA 134a中均不溶。PFOB和反向乳液在两种推进剂中均能以各种比例完全溶解或分散。本研究还证明反向FC乳液可成功用于以均匀且可重复的方式递送咖啡因。在包装后以及在室温下储存1周后,立即对压力罐中乳液水滴的平均直径进行了研究。乳液/推进剂比例在2/3至3/2之间且以HFA 227作为推进剂时获得了最佳结果。

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