» Articles » PMID: 36838565

A "Trojan Horse" Strategy: The Preparation of Bile Acid-Modifying Irinotecan Hydrochloride Nanoliposomes for Liver-Targeted Anticancer Drug Delivery System Study

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2023 Feb 25
PMID 36838565
Authors
Affiliations
Soon will be listed here.
Abstract

The bile acid transport system is a natural physiological cycling process between the liver and the small intestine, occurring approximately 6-15 times during the day. There are various bile acid transporter proteins on hepatocytes that specifically recognize bile acids for transport. Therefore, in this paper, a novel liposome, cholic acid-modified irinotecan hydrochloride liposomes (named CA-CPT-11-Lip), was prepared based on the "Trojan horse" strategy. The liposomes preparation process was optimized, and some important quality indicators were investigated. The distribution of irinotecan hydrochloride in mice was then analyzed by high-performance liquid chromatography (HPLC), and the toxicity of liposomes to hepatocellular carcinoma cells (HepG-2) was evaluated in vitro. As a result, CA-CPT-11-Lip was successfully prepared. It was spherical with a particle size of 154.16 ± 4.92 nm, and the drug loading and encapsulation efficiency were 3.72 ± 0.04% and 82.04 ± 1.38%, respectively. Compared with the conventional liposomes (without cholic acid modification, named CPT-11-Lip), CA-CPT-11-Lip had a smaller particle size and higher encapsulation efficiency, and the drug accumulation in the liver was more efficient, enhancing the anti-hepatocellular carcinoma activity of irinotecan hydrochloride. The novel nanoliposome modified by cholic acid may help to expand the application of irinotecan hydrochloride in the treatment of hepatocellular carcinoma and construct the drug delivery system mode of drug liver targeting.

Citing Articles

A Novel Delivery System for the Combined Use of Natural Ingredients: The Preparation of Berberine Hydrochloride-Matrine Liposomes and Preliminary Exploration of Their Anti-Tumor Activity.

Xu M, Ye Z, Liu J, Zhu S, Chen Y, Cai J Molecules. 2024; 29(21).

PMID: 39519850 PMC: 11547310. DOI: 10.3390/molecules29215210.


Nanoliposomes Permeability in a Microfluidic Drug Delivery Platform across a 3D Hydrogel.

Peyret C, Manousaki A, Bouguet-Bonnet S, Stratakis E, Sanchez-Gonzalez L, Kahn C Pharmaceutics. 2024; 16(6).

PMID: 38931887 PMC: 11207390. DOI: 10.3390/pharmaceutics16060765.


Targeted Nanoparticles: the Smart Way for the Treatment of Colorectal Cancer.

Abdellatif A, Alshubrumi A, Younis M AAPS PharmSciTech. 2024; 25(1):23.

PMID: 38267656 DOI: 10.1208/s12249-024-02734-9.

References
1.
Chamseddine A, Ducreux M, Armand J, Paoletti X, Satar T, Paci A . Intestinal bacterial β-glucuronidase as a possible predictive biomarker of irinotecan-induced diarrhea severity. Pharmacol Ther. 2019; 199:1-15. DOI: 10.1016/j.pharmthera.2019.03.002. View

2.
Seyfried T, Huysentruyt L . On the origin of cancer metastasis. Crit Rev Oncog. 2012; 18(1-2):43-73. PMC: 3597235. DOI: 10.1615/critrevoncog.v18.i1-2.40. View

3.
Javed Ansari M, Rahman M, Alharbi K, Altowayan W, Ali A, Almalki W . Hispolon-Loaded Liquid Crystalline Nanoparticles: Development, Stability, In Vitro Delivery Profile, and Assessment of Hepatoprotective Activity in Hepatocellular Carcinoma. ACS Omega. 2022; 7(11):9452-9464. PMC: 8945187. DOI: 10.1021/acsomega.1c06796. View

4.
Yamada Y, Fujii H, Ohata K, Kato-Hayashi H, Watanabe D, Ishihara T . High total bilirubin level is a significant risk factor for severe neutropenia in patients receiving irinotecan-based chemotherapy. Med Oncol. 2019; 36(7):63. DOI: 10.1007/s12032-019-1288-7. View

5.
Nayak D, Boxi A, Ashe S, Thathapudi N, Nayak B . Stavudine loaded gelatin liposomes for HIV therapy: Preparation, characterization and in vitro cytotoxic evaluation. Mater Sci Eng C Mater Biol Appl. 2017; 73:406-416. DOI: 10.1016/j.msec.2016.12.073. View