journal article·2024-02-11

Characterization of isoniazid incorporation into chitosan-poly(aspartic acid) nanoparticles

Carmen L. Zegarra-Urquia, Julio Santiago, Joel D. Bumgardner, Alexander K. Goroncy, José Vega-Baudrit, Claudia A. Hernández-Escobar, E. Armando Zaragoza-Contreras

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Abstract

The incorporation of the drug Isoniazid (an anti-tuberculosis drug) into nanoparticles of polyelectrolyte chitosan-poly(aspartic acid) complexes was carried out by the ionotropic gelation technique, adding a sodium polyaspartate solution containing the drug to a chitosan solution in different proportions in a mass ratio (mg/mg) Isoniazid/Chitosan. This was confirmed by MALDI-TOF/MS, ESI/MS, FTIR, and UV-Vis. The lowest average particle diameter (PD), estimated by DSL, was 148.5 ± 1 nm corresponding to an Isoniazid/chitosan ratio (mg/mg) of 0.5:1. FE-SEM showed nanoparticles in the order of 100–300 nm; whereas AFM showed semi-spherical particle morphology.
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Research context

OpenAlex topics: Advanced Drug Delivery Systems · Surfactants and Colloidal Systems · Polymer Surface Interaction Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Departamento de Química Orgánica, Universidad Nacional Mayor de San Marcos, Lima, Peru

Biomedical Engineering, The University of Memphis, Memphis, Tennessee, USA

Department of Chemistry, University of Wyoming, Laramie, Wyoming, USA

Centro Nacional de Alta Tecnología “Dr. Franklin Chang Díaz”, Laboratorio Nacional de Nanotecnología (LANOTEC), San José, Costa Rica

POLIUNA, Escuela de Química, Universidad Nacional, Heredia, Costa Rica

Department of Engineering and Materials Chemistry, Centro de Investigación en Materiales Avanzados, Complejo Industrial Chihuahua, Chihuahua, Mexico

References (48)

Show source-provided references
1. 10.3109/02652048.2011.59943710.3109/02652048.2011.599437 ↗
2. 10.1056/nejmra120089410.1056/nejmra1200894 ↗
3. 10.1016/j.ijregi.2022.01.00410.1016/j.ijregi.2022.01.004 ↗
4. 10.18433/j3m59p10.18433/j3m59p ↗
5. 10.1016/j.imu.2022.10084910.1016/j.imu.2022.100849 ↗
6. 10.1183/09031936.0007730710.1183/09031936.00077307 ↗
7. 10.2174/13895570778233174010.2174/138955707782331740 ↗
8. 10.1016/j.ijid.2021.03.09310.1016/j.ijid.2021.03.093 ↗
9. 10.3109/21691401.2015.100850810.3109/21691401.2015.1008508 ↗
10. 10.4103/0253-7613.7188710.4103/0253-7613.71887 ↗
11. 10.2174/221173850666618062512003810.2174/2211738506666180625120038 ↗
12. 10.1002/1521-4184(200106)334:6<189::AID-ARDP189>3.0.CO;2-610.1002/1521-4184(200106)334:6<189::AID-ARDP189>3.0.CO;2-6 ↗
13. 10.4314/tjpr.v6i4.1466510.4314/tjpr.v6i4.14665 ↗
14. 10.1016/j.tube.2003.07.00110.1016/j.tube.2003.07.001 ↗
15. 10.1093/jac/dkl12810.1093/jac/dkl128 ↗
16. Pandey, R.; Sharma, S.; Khuller, G. K. Oral Poly(Lactide-co-Glycolide) Nanoparticle Based Antituberculosis Drug Delivery: Toxicological and Chemotherapeutic Implications. Indian J. Exp. Biol. 2006, 44, 459–467.
17. 10.1093/jac/dkh41110.1093/jac/dkh411 ↗
18. 10.1016/j.colsurfb.2012.12.00810.1016/j.colsurfb.2012.12.008 ↗
19. 10.1021/acsabm.9b0000310.1021/acsabm.9b00003 ↗
20. 10.1016/j.eurpolymj.2013.06.02010.1016/j.eurpolymj.2013.06.020 ↗
21. 10.1016/j.ijbiomac.2020.10.19210.1016/j.ijbiomac.2020.10.192 ↗
22. 10.1080/00914037.2022.202944010.1080/00914037.2022.2029440 ↗
23. 10.1021/ja990276a10.1021/ja990276a ↗
24. 10.1002/hlca.20170016610.1002/hlca.201700166 ↗
25. 10.1021/ol010036b10.1021/ol010036b ↗
26. 10.1016/j.progpolymsci.2005.12.00110.1016/j.progpolymsci.2005.12.001 ↗
27. 10.1016/j.ijpharm.2008.04.04210.1016/j.ijpharm.2008.04.042 ↗
28. 10.3390/polym1112201010.3390/polym11122010 ↗
29. 10.1021/ac035331j10.1021/ac035331j ↗
30. 10.1002/rcm.321910.1002/rcm.3219 ↗
31. 10.1042/bj126044910.1042/bj1260449 ↗
32. 10.1016/S1472-9792(08)70011-810.1016/S1472-9792(08)70011-8 ↗
33. 10.1007/s00396-007-1785-710.1007/s00396-007-1785-7 ↗
34. 10.1007/s13361-011-0150-810.1007/s13361-011-0150-8 ↗
35. 10.1016/S1044-0305(01)00230-610.1016/S1044-0305(01)00230-6 ↗
36. 10.2298/JSC110201145D10.2298/JSC110201145D ↗
37. 10.1590/0074-0276014045810.1590/0074-02760140458 ↗
38. 10.5897/AJPP2014.419710.5897/AJPP2014.4197 ↗
39. 10.1080/10242422.2017.129523110.1080/10242422.2017.1295231 ↗
40. 10.1016/j.ijbiomac.2018.09.19410.1016/j.ijbiomac.2018.09.194 ↗
41. 10.1016/j.polymertesting.2011.02.00710.1016/j.polymertesting.2011.02.007 ↗
42. Hebda E.; Pielichowski J. A. N. Poly (Aspartic Acid) – Based Catalysts for the Oxidation Reactions Zastosowanie Katalizatorów Na Bazie Poli (Kwasu Asparaginowego) W Reakcjach Utleniania. Czas Tech Chem 2008.
43. 10.1021/jp903791410.1021/jp9037914 ↗
44. 10.1016/j.jsps.2020.10.00810.1016/j.jsps.2020.10.008 ↗
45. 10.1016/j.eurpolymj.2021.11076710.1016/j.eurpolymj.2021.110767 ↗
46. 10.3390/pharmaceutics1212119610.3390/pharmaceutics12121196 ↗
47. 10.1016/B978-0-323-46143-6.00022-110.1016/B978-0-323-46143-6.00022-1 ↗
48. 10.1515/epoly-2021-008510.1515/epoly-2021-0085 ↗