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Improved Therapeutic Efficacy of MT102, a New Anti-Inflammatory Agent, via a Self-Microemulsifying Drug Delivery System, in Ulcerative Colitis Mice.
Baral, Kshitis Chandra; Lee, Sang Hoon; Song, Jae Geun; Jeong, Seong Hoon; Han, Hyo-Kyung.
Afiliación
  • Baral KC; College of Pharmacy, Dongguk University-Seoul, Goyang 10326, Republic of Korea.
  • Lee SH; College of Pharmacy, Dongguk University-Seoul, Goyang 10326, Republic of Korea.
  • Song JG; College of Pharmacy, Dongguk University-Seoul, Goyang 10326, Republic of Korea.
  • Jeong SH; College of Pharmacy, Dongguk University-Seoul, Goyang 10326, Republic of Korea.
  • Han HK; College of Pharmacy, Dongguk University-Seoul, Goyang 10326, Republic of Korea.
Pharmaceutics ; 15(12)2023 Dec 02.
Article en En | MEDLINE | ID: mdl-38140061
ABSTRACT
MT-102 is a new anti-inflammatory agent derived from Juglans mandshurica and Isatis indigotica. Its therapeutic potential is hindered by low aqueous solubility, impacting its in vivo efficacy. Therefore, this study aimed to develop a self-microemulsifying drug delivery system (SMEDDS) for MT-102 to enhance its oral efficacy in treating ulcerative colitis. Solubility assessment in different oils, surfactants, and cosurfactants led to a SMEDDS formulation of MT-102 using Capmul MCM, Tween 80, and propylene glycol. Based on a pseudoternary phase diagram, the optimal SMEDDS composition was selected, which consisted of 15% Capmul MCM, 42.5% Tween 80, and 42.5% propylene glycol. The resulting optimized SMEDDS (SMEDDS-F1) exhibited a narrow size distribution (177.5 ± 2.80 nm) and high indirubin content (275 ± 5.58 µg/g, a biomarker). Across an acidic to neutral pH range, SMEDDS-F1 showed rapid and extensive indirubin release, with dissolution rates approximately 15-fold higher than pure MT-102. Furthermore, oral administration of SMEDDS-F1 effectively mitigated inflammatory progression and symptoms in a mouse model of ulcerative colitis, whereas pure MT-102 was ineffective. SMEDDS-F1 minimized body weight loss (less than 5%) without any significant change in colon length and the morphology of colonic tissues, compared to those of the healthy control group. In addition, oral administration of SMEDDS-F1 significantly inhibited the secretion of pro-inflammatory cytokines such as IL-6 and TNF-α. In conclusion, the SMEDDS-F1 formulation employing Capmul MCM, Tween 80, and propylene glycol (1542.542.5, w/w) enhances the solubility and therapeutic efficacy of MT-102.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article Pais de publicación: Suiza