Preparation and Evaluation of Stability and Acute Oral Toxicity of a Drug Delivery System Combining MIL‐100(Fe) with Chloroquine Phosphate

氯喹 急性毒性 药品 药物输送 药理学 磷酸盐 毒性 医学 化学 内科学 疟疾 病理 生物化学 有机化学
作者
Bac Thanh Le,Chau Que Nguyen,Ha Duc Ninh,Hoai Phuong Nguyen Thi,Duong Duc La,Hoai Phuong Nguyen Thi
出处
期刊:ChemistrySelect [Wiley]
卷期号:9 (39)
标识
DOI:10.1002/slct.202402854
摘要

Abstract Metal‐organic framework materials (MOFs) are highly porous and are the subject of growing interest among scientists globally for their utilization in drug delivery. In this work, iron‐based metal‐organic frameworks (MOFs) MIL‐100(Fe) were synthesized by ultrasonic method and studied for the loading of the chloroquine phosphate (CQP). The CQP‐release behavior of the material was investigated in water media with various pH solutions of 1.2, 2, 4.5, and phosphate‐buffered saline (PBS) at temperatures of 25 °C to 45 °C. MIL‐100(Fe) material had a high surface area of up to 1080 m 2 /g and could completely release the CQP at a pH of 1.2 after 25 hours. At other pH conditions, the drug exhibited an initial rapid release, followed by a gradual slowdown, ultimately achieving complete release after 96 hours. The maximal loading capacity for the CQP by the MIL‐100(Fe) was determined to be approximately 30 % at the pH solution of 2 (stomach environment). The findings from the activity assessment against the K1 malaria parasite strain (P. falciparum) indicated that the concentration at which the active ingredient, when carried by the material, exhibited inhibition was 193 nM/L. The evaluation outcomes for acute toxicity of the drug carrier material revealed an LD50 value exceeding 5000 mg/kg (equivalent to 1500 mg of CQP base). In contrast, when using the active substance alone, acute toxicity resulted in an LD50 value of 675 mg/kg.

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