Formulation development, characterization, and evaluation of bedaquiline fumarate - Soluplus® - solid dispersion.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmaceutical Development and Technology Pub Date : 2024-06-01 Epub Date: 2024-05-10 DOI:10.1080/10837450.2024.2348585
Vishwas P Pardhi, Manisha Patel, Keerti Jain
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Abstract

Bedaquiline fumarate (BQF) is classified as a BCS class II drug and has poor water solubility and dissolution rate, which ultimately compromises bioavailability. The objective of this study is to improve the biopharmaceutical properties of BQF through a solid dispersion system by using Soluplus®. Two solid dispersion systems were prepared i.e. binary solid dispersion (BSD) and ternary solid dispersion (TSD) where 14.31-fold and 20.43-fold increase in solubility of BQF was observed with BSD and TSD in comparison to BQF. In our previous research work, we explored the BSD and TSD of BQF with a crystalline polymer, poloxamer 188, which showed an increment in the solubility of BQF. In the current research, amorphous Soluplus® polymer was selected to formulate BSD and TSD with BQF and showed higher solubility than poloxamer 188. The various solid and liquid state characterization results confirmed the presence of an amorphous form of BQF inside solid dispersion. The Fourier transform infrared spectroscopy showed no chemical interactions between BQF and polymer. The cellular uptake results demonstrated higher uptake in Caco-2 cell lines. Pharmacokinetic studies showed enhanced solubility and bioavailability of TSDs. Hence, the present research shows a promising formulation strategy for enhancing the biopharmaceutical performance of BQF by increasing its solubility.

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富马酸贝达喹啉 -Soluplus® - 固体分散剂的配方开发、表征和评估。
富马酸贝达喹啉(BQF)被列为 BCS II 类药物,水溶性和溶解速率较差,最终影响了生物利用度。本研究的目的是使用 Soluplus® 通过固体分散体系改善 BQF 的生物药学特性。我们制备了两种固体分散体系,即二元固体分散体系(BSD)和三元固体分散体系(TSD),与 BQF 相比,BSD 和 TSD 的 BQF 溶解度分别提高了 14.31 倍和 20.43 倍。在我们之前的研究工作中,我们探索了 BQF 与结晶聚合物 Poloxamer 188 的 BSD 和 TSD,结果表明 BQF 的溶解度有所提高。在当前的研究中,我们选择了无定形的 Soluplus ® 聚合物来配制 BQF 的 BSD 和 TSD,结果表明其溶解度高于 poloxamer 188。各种固态和液态表征结果证实,在固体分散体中存在无定形形式的 BQF。傅立叶变换红外光谱显示,BQF 与聚合物之间没有化学作用。细胞吸收结果表明,Caco-2 细胞系的吸收率较高。药代动力学研究表明,TSDs 的溶解度和生物利用度均有所提高。因此,本研究表明,通过提高 BQF 的溶解度来增强其生物制药性能是一种很有前景的配方策略。
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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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