Chitosan-TPP microcapsules for controlled drug release

被引:1
作者
Perez-Pacheco, Yaride [1 ]
Alimandi, Tiziano [3 ]
Tylkowski, Bartosz [1 ]
Sistere, Miquel [2 ]
Garcia-Valls, Ricard [1 ]
机构
[1] Univ Rovira i Virgili, Chem Engn Dept, Av Paisos Catalans 18, Tarragona 43073, Spain
[2] Sisvilab, Prat de la Riba 63,1,2, Lleida 25004, Spain
[3] Tuscia Univ, Via Santa Maria Gradi 4, I-01100 Viterbo, VT, Italy
关键词
CS/TPP complexes; spray dryer; micro-; capsules; NANOPARTICLES;
D O I
10.55815/424214
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Production of chitosan/sodium tripolyphosphate (CS/ TPP) microcapsules via spray drying involves atomizing an emulsion containing CS, TPP, acetic acid (AcOH), and folic acid (FA) into fine droplets exposed to hightemperature, low-pressure gas flow. Solvent evaporation within the drying chamber leads to solid particle formation. Spray drying is valuable for creating solid CS/TPP microcapsules. Precise equipment parameter adjustments, like inlet temperature and gas flow rate, enable the study of microcapsule morphology, size, and properties. This adaptability allows for customization to specific pH dissolution ranges. The production method's impact on CS/TPP microcapsules was studied by modifying spray drier parameters, including inlet temperature and aspirator pressure, to enhance understanding of their behavior in solution under varied production conditions. In chitosan delivery systems, various approaches can encapsulate drug agents like folic acid, an analog to the cancer treatment drug methotrexate. Agents can be added to the chitosan solution pre-crosslinking, incorporated into gelation -inducing agents pre -mixing with chitosan, or included in the crosslinking mixture. Experiments were conducted to assess CS/TPP microcapsules' behavior when encapsulating agents like folic acid. Release profiles were analyzed to understand their drug delivery capabilities and potential as controlled release carriers.
引用
收藏
页码:33 / 42
页数:11
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