NMR relaxation and diffusion studies to probe the motional dynamics of risperidone within PLGA microsphere

IF 1.7
Deepak Kumar , Samanwita Pal
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Abstract

The present study aims to investigate the motional dynamics of risperidone within polylactic co-glycolic acid (PLGA) microsphere by employing solution state 1H and 19F nuclear magnetic resonance (NMR) measurements. Risperidone, a second-generation fluorinated antipsychotic drug used for the treatment of schizophrenia is commercially marketed as PLGA microsphere formulation resulting in prolonged release of the drug in solution. Although the current trend in the pharmaceutical market is to develop drug formulation with long-acting release (LAR) products, complete physicochemical characterization of such formulations are scarce. Especially the effects of microsphere encapsulation on the motional properties and diffusion behavior of the drugs are not discussed adequately in any of the earlier reports. We therefore, have employed NMR relaxation and diffusion measurements to decipher the interaction of PLGA cavity water with risperidone. A detailed analysis of NMR relaxation rates confirmed the event of encapsulation and the presence of local motion in the non-fluorinated end of risperidone. Further, the relaxation data indicated a significant alteration in 19F chemical shift anisotropy (CSA) and CSA/dipole-dipole (DD) cross-correlated relaxation mechanism and decreased effect of solvent relaxation pointing out reduced water concentration within the microsphere cavity. 1H and 19F diffusion coefficients of risperidone led to the information about hydrodynamic radius of risperidone in free and encapsulated states. Measurement of hydrodynamic radius supported the presence of limited water in PLGA cavity allowing higher translational mobility of risperidone after the encapsulation.

Abstract Image

核磁共振弛豫和扩散研究利培酮在PLGA微球内的运动动力学
本研究旨在利用1H和19F核磁共振(NMR)测量溶液状态,研究利培酮在聚乳酸共乙醇酸(PLGA)微球中的运动动力学。利培酮是一种用于治疗精神分裂症的第二代氟化抗精神病药物,在商业上以PLGA微球制剂销售,导致药物在溶液中释放时间延长。尽管目前制药市场的趋势是开发具有长效释放(LAR)产品的药物制剂,但对此类制剂进行完整的物理化学表征的研究很少。特别是微球包封对药物运动特性和扩散行为的影响,在以往的报道中没有得到充分的讨论。因此,我们采用核磁共振弛豫和扩散测量来破译PLGA空腔水与利培酮的相互作用。对核磁共振弛豫率的详细分析证实了利培酮非氟端包封和局部运动的存在。此外,弛豫数据表明,微球腔内的19F化学位移各向异性(CSA)和CSA/偶极子-偶极子(DD)交叉相关弛豫机制发生了显著变化,溶剂弛豫效应减弱,表明微球腔内水浓度降低。利培酮的1H和19F扩散系数给出了利培酮在游离和包封状态下的水动力半径信息。水动力半径的测量支持PLGA腔中存在有限的水,从而使利培酮在包封后具有更高的平移迁移率。
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来源期刊
Magnetic Resonance Letters
Magnetic Resonance Letters Analytical Chemistry, Spectroscopy, Radiology and Imaging, Biochemistry, Genetics and Molecular Biology (General)
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