Design and optimization of DPC-crosslinked HPβCD nanosponges for entrectinib oral delivery: formulation, characterization, and pharmacokinetic studies

IF 3.4 Q2 PHARMACOLOGY & PHARMACY Future Journal of Pharmaceutical Sciences Pub Date : 2024-08-14 DOI:10.1186/s43094-024-00680-8
Konda Sri Chaya Reddy, Darna Bhikshapathi
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Abstract

Background

In advanced or metastatic cancers characterized by specific genetic alterations, heightened growth and resistance to conventional therapies are common. Targeted treatments like entrectinib (ENT) precisely inhibit aberrant signaling pathways, potentially enhancing outcomes. The objective of this research is to develop and enhance the effectiveness of entrectinib-loaded nanosponge formulations by utilizing hydroxypropyl-β-cyclodextrin (HPβCD) to improve its oral bioavailability.

Results

The study employed surface response methodology and Design-Expert® software to optimize key formulation variables such as the molar concentration ratio of the polymer and cross-linker, as well as process variables such as stirring speed and duration. Optimization focused on particle size, polydispersity index, and percentage entrapment efficiency. Validation methods encompassed Fourier transform spectroscopy (FTIR), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), in vitro release studies, and in vivo studies.

After optimization, ENT-loaded HPβCD NSPs were formulated with a molar ratio (P:CL) of 0.800 mg, stirred at 3000 rpm for 420 min, achieving a desirability of 0.926. Predicted values for PS (particle size), PdI (polydispersity index), and EE % (entrapment efficiency) were 146.98 nm, 0.263, and 88.29%, respectively. The optimized formulation showed a mean size of 151.8 ± 5.6 nm, PDI of 0.233 ± 0.049, and EE of 87.36 ± 1.61%. Further validation through various analyses confirmed the optimization's efficacy, with notable improvements demonstrated in AUC0-t (6.30-fold) and Cmax (4.10 times) compared to the free drug.

Conclusion

The findings of the study indicated that nanosponges exhibit promise as an effective carrier for delivering entrectinib, addressing for advance tumor effectively by enhancing release and bioavailability in the treatment of cancer.

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设计和优化用于口服给药 Entrectinib 的 DPC 交联 HPβCD 纳米海绵:配方、表征和药代动力学研究
背景在以特定基因改变为特征的晚期或转移性癌症中,生长加快和对传统疗法产生抗药性是常见现象。entrectinib(ENT)等靶向治疗可精确抑制异常信号通路,从而提高治疗效果。本研究的目的是利用羟丙基-β-环糊精(HPβCD)开发并提高entrectinib负载纳米海绵制剂的有效性,以改善其口服生物利用度。结果该研究采用了表面响应方法学和Design-Expert®软件来优化聚合物和交联剂的摩尔浓度比等关键制剂变量以及搅拌速度和持续时间等工艺变量。优化的重点是粒度、多分散指数和夹带效率百分比。验证方法包括傅立叶变换光谱法(FTIR)、差示扫描量热法(DSC)、扫描电子显微镜(SEM)、体外释放研究和体内研究。经过优化,ENT负载的HPβCD NSP的摩尔比(P:CL)为0.800毫克,在3000转/分钟的转速下搅拌420分钟,达到0.926的理想值。PS(粒度)、PdI(多分散指数)和 EE %(夹带效率)的预测值分别为 146.98 nm、0.263 和 88.29%。优化配方的平均粒度为 151.8 ± 5.6 nm,PDI 为 0.233 ± 0.049,EE 为 87.36 ± 1.61%。该研究结果表明,纳米海绵有望成为输送恩替利尼的有效载体,通过提高释放和生物利用度来有效推进肿瘤的治疗。
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来源期刊
自引率
0.00%
发文量
44
审稿时长
23 weeks
期刊介绍: Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.
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