Guru Gobind Singh College of Pharmacy, Yamuna Nagar-135001, Haryana, India.
Department of Pharmaceutics, MM College of Pharmacy, MM (DU), Mullana, Ambala, Haryana, India.
Curr Drug Deliv. 2024;21(10):1422-1432. doi: 10.2174/0115672018261505231018100329.
Although nucleation kinetic data is quite important for the concept of supersaturation behavior, its part in rationalizing the crystallization inhibitor has not been well understood.
This study aimed to investigate the nucleation kinetic profile of Dextromethorphan HBr (as an ideal drug, BCS-II) by measuring liquid-liquid phase segregation, nucleation induction time, and Metastable Zone width.
Surfeit action was examined by a superfluity assay of the drug. The concentration was scrutinized by light scattering techniques (UV spectrum (novel method) and Fluorometer (CL 53)).
The drug induction time was 20 min without polymer and 90 and 110 min with polymers, such as HPMC K15M and Xanthan Gum, respectively. Therefore, the order of the polymer's ability to inhibit nucleation was Xanthan Gum > HPMC K15M in the medium (7.4 pH). Similarly, the drug induction time was 30 min without polymer and 20, 110, and 90 min with polymers, such as Sodium CMC, HPMC K15M, and Xanthan Gum, respectively. Therefore, the order of the polymer's ability to inhibit nucleation was HPMC K15M > Xanthan Gum > Sodium CMC in SIFsp (6.8 pH), which synchronizes the polymer's potentiality to interdict the drug precipitation.
The HPMC K15M and xanthan Gum showed the best crystallization inhibitor effect for the maintenance of superfluity conditions till the drug absorption time. The xanthan gum is based on the "glider" concept, and this shows the novelty of this preliminary research. The screening methodology used for rationalizing the best polymers used in the superfluity formulations development successfully.
尽管成核动力学数据对于过饱和度行为的概念非常重要,但人们对其在合理利用结晶抑制剂方面的作用还没有很好地理解。
本研究旨在通过测量液-液相分离、成核诱导时间和亚稳区宽度,来研究右美沙芬溴化物(作为一种理想的药物,BCS-II)的成核动力学特征。
通过药物过剩测定来检验超饱作用。通过光散射技术(紫外光谱(新方法)和荧光计(CL53))来检测浓度。
在没有聚合物的情况下,药物诱导时间为 20 分钟,而在聚合物 HPMC K15M 和黄原胶存在的情况下,诱导时间分别为 90 和 110 分钟。因此,聚合物抑制成核能力的顺序为黄原胶>HPMC K15M(在 pH7.4 的介质中)。同样,在没有聚合物的情况下,药物诱导时间为 30 分钟,而在聚合物如羧甲基纤维素钠、HPMC K15M 和黄原胶存在的情况下,诱导时间分别为 20、110 和 90 分钟。因此,聚合物抑制成核能力的顺序为 HPMC K15M>黄原胶>羧甲基纤维素钠(在 pH6.8 的 SIFsp 中),这与聚合物抑制药物沉淀的潜力一致。
HPMC K15M 和黄原胶在维持过剩条件直到药物吸收时间方面表现出最好的结晶抑制剂效果。黄原胶基于“滑翔器”的概念,这显示了这项初步研究的新颖性。用于合理选择用于过剩配方开发的最佳聚合物的筛选方法成功。