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提高生物利用度:口服异维 A 酸制剂的进展。

Enhancing Bioavailability: Advances in Oral Isotretinoin Formulations.

机构信息

Schulich School of Medicine and Dentistry, Western University, Windsor, ON, Canada.

出版信息

Skin Therapy Lett. 2024 Sep;29(5):10-12.

Abstract

Oral isotretinoin continues to be unsurpassed in efficacy for acne. However, it is associated with potential adverse events including risk of fetal defects, necessitating appropriate mitigation strategies. Furthermore, the variance in bioavailability of the original formulation when ingested in fed versus fasted conditions can lead to differences in daily dosing and duration of exposure. Advances in formulation, with lidose encapsulation and subsequently with micronization, have led to iterative improvements in reducing bioavailability variation between fed and fasted conditions. Differences in bioavailability during fasting were 60% less for originator oral isotretinoin, 33% less for lidose-encapsulated form, and 20% less for micronized-isotretinoin formulation. The latter also demonstrated overall greater bioavailability such that a 20% dose reduction was required compared to the originator and lidose-encapsulated formulations. By reducing the effect of high-fat/high calorie food co-ingestion, this micronized formulation may facilitate clarity in determining appropriate oral isotretinoin dose requirements in achieving optimal patient outcomes.

摘要

口服异维 A 酸在治疗痤疮方面的疗效仍然是无与伦比的。然而,它与潜在的不良反应有关,包括胎儿畸形的风险,因此需要采取适当的缓解策略。此外,口服异维 A 酸在进食和禁食条件下的生物利用度差异会导致每日剂量和暴露时间的差异。在配方方面的进展,包括 lidose 包封,随后进行微粉化,已经导致在减少进食和禁食条件下生物利用度差异方面的迭代改进。对于原研口服异维 A 酸,禁食期间的生物利用度差异降低了 60%,对于 lidose 包封形式降低了 33%,对于微粉化异维 A 酸制剂降低了 20%。后者还表现出总体更高的生物利用度,因此与原研药和 lidose 包封制剂相比,需要减少 20%的剂量。通过减少高脂肪/高卡路里食物共摄入的影响,这种微粉化制剂可能有助于明确确定实现最佳患者结果所需的口服异维 A 酸剂量要求。

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