4.6 Article

Preclinical evaluations of Norcantharidin liposome and emulsion hybrid delivery system with improved encapsulation efficiency and enhanced antitumor activity

期刊

EXPERT OPINION ON DRUG DELIVERY
卷 19, 期 4, 页码 451-464

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/17425247.2022.2063834

关键词

Norcantharidin; Liposomes; Emulsions; Hybrid delivery system; Antitumor activity

资金

  1. National Mega-project for Innovative Drugs [2019ZX09721001]
  2. Liaoning Revitalization Talents Program [XLYC1908031]
  3. National Science and Technology Major Project of the Ministry of Science and Technology of China [2018ZX09735005]
  4. Special Translational Project for Medical Scientific and Technological Achievements of Liaoning Province
  5. Shengjing Hospital of China Medical University [M0397]
  6. Liaoning Livelihood Science and Technology Plan Joint Project [2021JH2/10300130]

向作者/读者索取更多资源

In this study, a novel nanocarrier, NLEH, was developed to improve the encapsulation efficiency, sterilization stability, and antitumor activity of norcantharidin (NCTD). NLEH exhibited higher encapsulation efficiency and better sterilization stability compared to NCTD liposomes and NCTD emulsions. Furthermore, NLEH showed improved therapeutic effects by promoting absorption, prolonging blood circulation, enhancing tumor-targeting accumulation, improving tumor penetration, and increasing antitumor immunity.
Background Norcantharidin (NCTD) has a certain degree of hydrophilicity and poor lipophilicity, and has some side-effects, including short t(1/2), vascular irritation, cardiotoxicity, and nephrotoxicity, which bring difficulties for formulation research. In this study, we aim to develop a novel nanocarrier to improve encapsulation efficiency, increase sterilization stability, and enhance antitumor activity. Methods Phospholipid complexes methods were used for increasing the lipophilicity of norcantharidin (NCTD), then NCTD phospholipid complexes were not only loaded in the oil phase and oil-water interface surface, but also encapsulated in phospholipid bilayers to obtain NCTD liposome-emulsion hybrid (NLEH) delivery system. The in vitro cytotoxicity and apoptosis, in vivo tissue distribution, tumor penetration, heterotopic, and orthotopic antitumor studies were conducted to evaluate therapeutic effect. Results NLEH exhibited an improved encapsulation efficiency (89.3%) and a better sterilization stability, compared to NCTD liposomes and NCTD emulsions. NLEH can achieve a better antitumor activity by promoting absorption (1.93-fold), prolonging blood circulation (2.08-fold), enhancing tumor-targeting accumulation (1.19 times), improving tumor penetration, and increasing antitumor immunity. Conclusions The liposome-emulsion hybrid (LEH) delivery system was potential carrier for NCTD delivery, and LEH could open opportunities for delivery of poorly soluble anticancer drugs, especially drugs that are more hydrophilicity than lipophilicity.

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