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含纳米化拉莫三嗪产品用于鼻粉制剂的初步研究。

Preliminary study of nanonized lamotrigine containing products for nasal powder formulation.

作者信息

Gieszinger Péter, Csóka Ildikó, Pallagi Edina, Katona Gábor, Jójárt-Laczkovich Orsolya, Szabó-Révész Piroska, Ambrus Rita

机构信息

Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary.

出版信息

Drug Des Devel Ther. 2017 Aug 23;11:2453-2466. doi: 10.2147/DDDT.S138559. eCollection 2017.

Abstract

The nasal delivery of drugs offers a great alternative route to avoid adverse events and to increase patient compliance due to its advantageous properties. Besides nasal application, topical, systemic and central effects are also available. Nasal powders (NPs) have better adhesion due to the additive polymers that may be, eg, gelling or good wettability agents; thus, their bioavailability is better compared to the liquid formulations. Using nanoparticles, innovative and more efficient products can be achieved, which may lead to the improvement of different therapies. The aim of this study was to produce NP formulations containing lamotrigine (LAM) as interactive physical mixtures and nanosized LAM-based formulations. After risk assessment of the preliminary tests, the micrometric properties (particle size and morphology) and the structural properties (differential scanning calorimetry [DSC], X-ray powder diffraction [XRPD]) were investigated; thereafter, physicochemical properties (solubility, polarity) and in vitro dissolution and diffusion profiles were also examined. These product samples showed an appropriate particle size ranging 10-25 µm, while the particle size of LAM in the products was between 120 and 230 nm and the dissolved amount of drug was >60% after 5 minutes in these cases.

摘要

药物的鼻腔给药提供了一种很好的替代途径,由于其有利特性,可避免不良事件并提高患者的依从性。除鼻腔给药外,还可产生局部、全身和中枢作用。鼻用粉剂(NPs)由于添加了聚合物(例如可能是凝胶剂或具有良好润湿性的试剂)而具有更好的黏附性;因此,与液体制剂相比,它们的生物利用度更高。使用纳米颗粒可以实现创新且更高效的产品,这可能会改善不同的治疗方法。本研究的目的是制备含有拉莫三嗪(LAM)的NP制剂,作为相互作用的物理混合物和基于纳米尺寸LAM的制剂。在对初步试验进行风险评估后,研究了微米级特性(粒径和形态)和结构特性(差示扫描量热法[DSC]、X射线粉末衍射[XRPD]);此后,还研究了理化性质(溶解度、极性)以及体外溶出和扩散曲线。这些产品样品的粒径范围为10 - 25 µm,而产品中LAM的粒径在120至230 nm之间,在这些情况下,5分钟后药物的溶解量>60%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61e/5574602/9bccdb20c5c1/dddt-11-2453Fig1.jpg

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