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Combination of miR159 Mimics and Irinotecan Utilizing Lipid Nanoparticles for Enhanced Treatment of Colorectal Cancer.
Yang, Rulei; Liu, Yiran; Yang, Ning; Zhang, Tian; Hou, Jiazhen; He, Zongyan; Wang, Yutong; Sun, Xujie; Shen, Jingshan; Jiang, Hualiang; Xie, Yuanchao; Lang, Tianqun.
Affiliation
  • Yang R; School of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Liu Y; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
  • Yang N; Vigonvita Life Sciences Co., Ltd., Suzhou 215125, China.
  • Zhang T; Lingang Laboratory, Shanghai 200031, China.
  • Hou J; Lingang Laboratory, Shanghai 200031, China.
  • He Z; Lingang Laboratory, Shanghai 200031, China.
  • Wang Y; Lingang Laboratory, Shanghai 200031, China.
  • Sun X; Lingang Laboratory, Shanghai 200031, China.
  • Shen J; Lingang Laboratory, Shanghai 200031, China.
  • Jiang H; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
  • Xie Y; Lingang Laboratory, Shanghai 200031, China.
  • Lang T; School of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Pharmaceutics ; 16(4)2024 Apr 22.
Article in En | MEDLINE | ID: mdl-38675231
ABSTRACT
Colorectal cancer (CRC) ranks as the third most prevalent global malignancy, marked by significant metastasis and post-surgical recurrence, posing formidable challenges to treatment efficacy. The integration of oligonucleotides with chemotherapeutic drugs emerges as a promising strategy for synergistic CRC therapy. The nanoformulation, lipid nanoparticle (LNP), presents the capability to achieve co-delivery of oligonucleotides and chemotherapeutic drugs for cancer therapy. In this study, we constructed lipid nanoparticles, termed as LNP-I-V by microfluidics to co-deliver oligonucleotides miR159 mimics (VDX05001SI) and irinotecan (IRT), demonstrating effective treatment of CRC both in vitro and in vivo. The LNP-I-V exhibited a particle size of 118.67 ± 1.27 nm, ensuring excellent stability and targeting delivery to tumor tissues, where it was internalized and escaped from the endosome with a pH-sensitive profile. Ultimately, LNP-I-V significantly inhibited CRC growth, extended the survival of tumor-bearing mice, and displayed favorable safety profiles. Thus, LNP-I-V held promise as an innovative platform to combine gene therapy and chemotherapy for improving CRC treatment.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pharmaceutics Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pharmaceutics Year: 2024 Document type: Article Affiliation country: China
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