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A biocompatible bismuth based metal-organic framework as efficient light-sensitive drug carrier
Qingyan Zhang1, Yuanyuan Liu1, Zeyan Wang1
1State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, PR China.
Journal of Colloid and Interface Science
|March 18, 2022
Summary
Bismuth-based metal-organic frameworks (MOFs) show promise as light-sensitive drug carriers. SU-101, made of bismuth and ellagic acid, efficiently loads and releases ciprofloxacin under light.
Area of Science:
- Materials Science
- Nanotechnology
- Drug Delivery
Background:
- Bismuth-based metal-organic frameworks (MOFs) possess low toxicity and photoactivity.
- These properties make them suitable for light-sensitive drug delivery applications.
- Developing efficient drug carriers is crucial for targeted and controlled therapeutic interventions.
Purpose of the Study:
- To investigate the potential of a bismuth-based MOF, SU-101, as a light-sensitive drug carrier.
- To evaluate the loading capacity and light-induced release of ciprofloxacin (CIP) from SU-101.
- To explore the mechanism of drug release and the universality of SU-101 for other drugs.
Main Methods:
- Synthesis and characterization of SU-101 (bismuth and ellagic acid MOF).
- Loading of ciprofloxacin (CIP) into SU-101 and determination of loading ratio.
- Investigation of CIP release kinetics under light illumination.
- Analysis of the interaction mechanism between SU-101 and drug molecules using hydrogen bonding principles.
Main Results:
- SU-101 demonstrated a high ciprofloxacin loading ratio of 85.8%.
- Controlled release of CIP was achieved under light illumination, with a maximum release ratio of 95.56%.
- Hydrogen bonding between ellagic acid and ciprofloxacin was identified as the key mechanism for drug loading and light-triggered release.
Conclusions:
- SU-101 exhibits significant potential as an efficient light-sensitive drug carrier.
- The drug release mechanism is dependent on light-induced disruption of hydrogen bonds.
- SU-101 shows versatility for carrying other drugs (e.g., norfloxacin, amoxicillin, tetracycline, doxorubicin hydrochloride) that can form hydrogen bonds.

