Division of Pharmaceutical Sciences, College of Pharmacy, University of New Mexico, Albuquerque, NM, USA.
J Microencapsul. 2010;27(8):657-68. doi: 10.3109/02652041003739840.
In this study, novel biodegradable physically cross-linked hydrogel microparticles were developed and evaluated in-vitro as potential carriers for inhalation therapy. These hydrogel microparticles were prepared to be respirable (desired aerodynamic size) when dry and also designed to avoid the macrophage uptake (attain large swollen size once deposited in lung). The swellable microparticles, prepared using cryomilling, were based on Pluronic® F-108 in combination with PEG grafted onto both chitosan (Cs) and its N-phthaloyl derivative (NPHCs). Polymers synthesized in the study were characterized using EA, FTIR, 2D-XRD and DSC. Morphology, particle size, density, biodegradation and moisture content of the microparticles were quantified. Swelling characteristics for both drug-free and drug-loaded microparticles showed excellent size increases (between 700-1300%) and the release profiles indicated sustained release could be achieved for up to 20 days. The respirable microparticles showed drug loading efficiency up to 92%. The enzymatic degradation of developed microparticles started within the first hour and only ∼10% weights were remaining after 10 days. In conclusion, these respirable microparticles demonstrated promising in-vitro performance for potential sustained release vectors in pulmonary drug delivery.
在这项研究中,开发了新型可生物降解的物理交联水凝胶微球,并在体外进行了评估,作为吸入治疗的潜在载体。这些水凝胶微球在干燥时被制备成可吸入的(所需的空气动力学尺寸),并且被设计为避免巨噬细胞摄取(一旦沉积在肺部就会达到大的肿胀尺寸)。可溶胀的微球是通过冷冻研磨制备的,基于 Pluronic® F-108 与接枝在壳聚糖(Cs)及其 N-邻苯二甲酰基衍生物(NPHCs)上的 PEG 结合。研究中合成的聚合物使用 EA、FTIR、2D-XRD 和 DSC 进行了表征。微球的形态、粒径、密度、生物降解性和水分含量进行了定量分析。无载药和载药微球的溶胀特性均显示出优异的粒径增加(700-1300%),释放曲线表明可实现长达 20 天的持续释放。可吸入微球的药物载量效率高达 92%。开发的微球的酶降解在最初的 1 小时内开始,10 天后仅剩余约 10%的重量。总之,这些可吸入的微球在体外展示了有前途的性能,有望成为肺部药物输送中持续释放载体。