Kalepu Sandeep, Nekkanti Vijaykumar
Department of Pharmaceutical Technology, Shri Vishnu College of Pharmacy, Bhimavaram, Andhra Pradesh, India.
College of Pharmacy, Western University of Health Sciences, Pomona, CA, USA.
Drug Deliv Transl Res. 2016 Jun;6(3):319-32. doi: 10.1007/s13346-016-0283-1.
Although a large number of new drug molecules with varied therapeutic potentials have been discovered in the recent decade, yet most of them are still in developmental process. This can be attributed to the limited aqueous solubility which governs the bioavailability of such drug molecules. Hence, there is a requisite for a technology-based product (formulation) in order to overcome such issues without compromising on the therapeutic response. The purpose of this review is to provide an insight to the formulation of drug nanoparticles for enhancing solubility and dissolution velocity with concomitant enhancement in bioavailability. In the recent decade, nanonization has evolved from a concept to reality owing to its versatile applications, especially in the development of drugs having poor solubility. In this review, a relatively simple and scalable approach for the manufacture of drug nanoparticles and latest characterization techniques utilized to evaluate the drug nanoparticles are discussed. The drug nanoparticulate approach described herein provides a general applicability of the platform technology in designing a formulation for drugs associated with poor aqueous solubility.
尽管在最近十年中发现了大量具有不同治疗潜力的新药分子,但其中大多数仍处于研发过程中。这可归因于有限的水溶性,而水溶性决定了此类药物分子的生物利用度。因此,需要一种基于技术的产品(制剂),以便在不影响治疗反应的情况下克服此类问题。本综述的目的是深入了解药物纳米颗粒的制剂,以提高溶解度和溶解速度,并同时提高生物利用度。在最近十年中,由于其广泛的应用,尤其是在开发低溶解度药物方面,纳米化已从一个概念发展成为现实。在本综述中,讨论了一种相对简单且可扩展的药物纳米颗粒制造方法以及用于评估药物纳米颗粒的最新表征技术。本文所述的药物纳米颗粒方法为平台技术在设计低水溶性药物制剂方面提供了普遍适用性。