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EFFICIENT DRUG CARRIER FOR ACETYLSALICYLIC ACID FROM CHITOSAN-BASED COMPOSITES PREPARED WITH MONTMORILLONITE, CELLULOSE AND HYDROXYAPATITE

Year 2024, Volume: 25 Issue: 3, 368 - 379, 30.09.2024
https://doi.org/10.18038/estubtda.1428785

Abstract

In this study, chitosan-based hydroxyapatite/chitosan (HAP/CHI), cellulose/chitosan (CEL/CHI) and montmorillonite/chitosan (MMT/CHI) composites were synthesized and characterized by Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM) and Thermogravimetric Analysis (TGA). Acetylsalicylic acid (ASA) was used as a drug for loading and desorption studies to determine the release behavior of the synthesized composites. The maximum adsorption capacities (qe) were obtained as 251.5 mg/g, 197.7 mg/g and 288.95 mg/g for HAP/CHI, CEL/CHI and MMT/CHI, respectively. In vitro release studies of ASA from the composites HAP/CHI, CEL/CHI, and MMT/CHI were carried out phosphate buffer solution (PBS) and gastric juice (GJ). In the intestinal medium (PBS) controlled drug release continued for 72 hours (4320 minutes), and burst release was observed in the first 5 minutes in all composites. 19.16%, 47.15% and 37.32% of the active ingredient from HAP/CHI, CEL/CHI and MMT/CHI composites, respectively, were released in the first 5 minutes. After 5 minutes, the release slowed down and became more controlled for all three composites. At the end of the release, the highest releasing composite was CEL/CHI, with 95.77% ASA release. A total drug release of 87.48% was achieved with MMT/CHI and 87.37% with HAP/CHI. In the gastric environment (GJ) Controlled drug release continued for 72 hours (4320 minutes), and burst release was observed in the first 5 minutes in all composites. 52.51%, 72.30% and 44.87% of the active ingredient from HAP/CHI, CEL/CHI and MMT/CHI composites, respectively, were released in the first 5 minutes. After 5 minutes, the release slowed down and became more controlled for all three composites. At the end of the release, the highest releasing capacity was found with the CEL/CHI composite, with 96.05% ASA release. A total drug release of 93.26% was achieved with HAP/CHI and 84.89% with MMT/CHI.

Ethical Statement

The author(s) stated that there are no conflicts of interest regarding the publication of this article.

Project Number

22ADP087

Thanks

This study was supported by Eskisehir Technical University Scientific Research Projects Commission under Grant No: 22ADP087

References

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  • [6] Kumari S, Singh RP. Glycolic acid-functionalized chitosan–Co3O4–Fe3O4 hybrid magnetic nanoparticles-based nanohybrid scaffolds for drug-delivery and tissue engineering. J Mater Sci. 2013; 48: 1524–1532.
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  • [8] Yao AH, Li XD, Xiong L, Zeng JH, Xu J, Wang DP. Hollow hydroxyapatite microspheres/chitosan composite as a sustained delivery vehicle for rhBMP-2 in the treatment of bone defects. J Mater Sci: Mater Med. 2015; 26: 1-12.
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  • [14] Xing G, Shao L, Du Y, Tao H, Qi C. Citric acid crosslinked chitosan/poly(ethylene oxide) composite nanofibers fabricated by electrospinning and thermal treatment for controlled drug release. Cellulose. 2021; 28: 961–971.
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  • [18] Paul A, Augustine R, Hasan A, Zahid AA, Thomas S, Agatemor C, Ghosal K. Halloysite nanotube and chitosan polymer composites: Physicochemical and drug delivery properties. Journal of Drug Delivery Science and Technology. 2022; 72: 103380.
  • [19] Cicek Ozkan, B. Cellulose and chitosan biopolymer composites reinforced with graphene and their adsorption properties for basic blue 41. Cellulose. 2022; 29: 9637–9655.
  • [20] Bhagath S, Vivek A, Krishna VV, Mittal SS, Balachandran M. Synthesis and characteristics of MMT reinforced chitosan nanocomposite. Materials Today: Proceedings. 2021; 46: 4487–4492.
  • [21] Günister E, Pestreli D, Ünlü CH, Atıcı O, Güngör N. Synthesis and characterization of chitosan-MMT biocomposite systems. Carbohydrate Polymers. 2007; 67: 358–365.
  • [22] Paluszkiewicz C, Stodolak E, Hasik M & Blazewicz, M. FT-IR study of montmorillonite–chitosan nanocomposite materials. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2011; 79(4): 784-788.
  • [23] Mohammed ASY, Dyab AK, Taha F, Abd El-Mageed, A. I. Pollen-derived microcapsules for aspirin microencapsulation: in vitro release and physico-chemical studies. RSC advances. 2022; 12(34): 22139-22149.
  • [24] Ravi Sankar V, Dachinamoorthi D, Chandra Shekar KB. A Comparative Pharmacokinetic study of Aspirin Suppositories and Aspirin Nanoparticles Loaded Suppositories. Clinic Pharmacol Biopharm. 2012; 1(105): 2.
  • [25] Vyskočilová E, Luštická I, Paterová I, Machová L, Červený L. Modified MCM-41 as a drug delivery system for acetylsalicylic acid. Solid state sciences. 2014; 38: 85-89.
  • [26] Dong LE, Gou G, Jiao L. Characterization of a dextran–coated layered double hydroxide acetylsalicylic acid delivery system and its pharmacokinetics in rabbit. Acta Pharmaceutica Sinica B. 2013; 3(6): 400-407.
Year 2024, Volume: 25 Issue: 3, 368 - 379, 30.09.2024
https://doi.org/10.18038/estubtda.1428785

Abstract

Project Number

22ADP087

References

  • [1] Ordikhani F, Dehghani M, Simchi A. Antibiotic-loaded chitosan–Laponite films for local drug delivery by titanium implants: cell proliferation and drug release studies. J Mater Sci: Mater Med. 2015; 26: 1-12.
  • [2] Parhi R. Chitin and Chitosan in Drug Delivery. In: Crini, G. and Lichtfouse, E. (eds.) Sustainable Agriculture Reviews 36: Chitin and Chitosan: Applications in Food, Agriculture, Pharmacy, Medicine and Wastewater Treatment. Springer International Publishing, 2019; 175–239.
  • [3] Shi J, Zhao H, Wu F, Gan X. Synthesis and characterization of an injectable rifampicin-loaded chitosan/hydroxyapatite bone cement for drug delivery. Journal of Materials Research. 2021; 36: 487–498.
  • [4] He M, Chen H, Zhang X, Wang C, Xu C, Xue Y, Wang J, Zhou P, Zhao Q.: Construction of novel cellulose/chitosan composite hydrogels and films and their applications. Cellulose. 2018; 25: 1987–1996.
  • [5] Küçükçalik A, Ünlü CH. Chitosan-Graft-Polyacrylamide Based Release Systems: Effect of pH and Crosslinking. Journal of the Turkish Chemical Society Section A: Chemistry. 2022; 9: 121–130.
  • [6] Kumari S, Singh RP. Glycolic acid-functionalized chitosan–Co3O4–Fe3O4 hybrid magnetic nanoparticles-based nanohybrid scaffolds for drug-delivery and tissue engineering. J Mater Sci. 2013; 48: 1524–1532.
  • [7] Liu X, Zhao X, Liu Y, Zhang T. Review on preparation and adsorption properties of chitosan and chitosan composites. Polym. Bull. 2022; 79: 2633–2665.
  • [8] Yao AH, Li XD, Xiong L, Zeng JH, Xu J, Wang DP. Hollow hydroxyapatite microspheres/chitosan composite as a sustained delivery vehicle for rhBMP-2 in the treatment of bone defects. J Mater Sci: Mater Med. 2015; 26: 1-12.
  • [9] Baştan FE. Production and characterization of gelatin functionalized hydroxyapatite composite microspheres for biomedical applications. Eskişehir Technical University Journal of Science and Technology A-Applied Sciences and Engineering. 2021; 22: 10–22.
  • [10] Sharifzadeh G, Hezaveh H, Muhamad, II, Hashim S, Khairuddin N. Montmorillonite-based polyacrylamide hydrogel rings for controlled vaginal drug delivery. Materials Science and Engineering: C. 2020; 110: 110609.
  • [11] Bekaroğlu MG, Nurili F, İşçi S. Montmorillonite as imaging and drug delivery agent for cancer therapy. Applied Clay Science. 2018; 162: 469–477.
  • [12] Haerudin H, Pramono AW, Kusuma DS, Jenie A, Voelcker NH, Gibson C. Preparation and characterization of chitosan/montmorillonite (mmt) nanocomposite systems. 2010. PhD Thesis. University of Indonesia.
  • [13] Sezer D, Hoşgün EZ. Controlled release of acetylsalicylic acid via hydroxyapatite prepared with different templates. J Aust Ceram Soc. 2023; 59: 153–163.
  • [14] Xing G, Shao L, Du Y, Tao H, Qi C. Citric acid crosslinked chitosan/poly(ethylene oxide) composite nanofibers fabricated by electrospinning and thermal treatment for controlled drug release. Cellulose. 2021; 28: 961–971.
  • [15] Li H, Ke J, Li H, Wei C, Wu X, Li J, Yang Y, Xu L, Liu H, Li S. Mesoporous silicas templated by heterocyclic amino acid derivatives: Biomimetic synthesis and drug release application. Materials Science and Engineering: C. 2018; 93: 407–418.
  • [16] Cheng ZH, Yasukawa A, Kandori K, Ishikawa T. FTIR Study of Adsorption of CO2 on Nonstoichiometric Calcium Hydroxyapatite. Langmuir. 1998; 14: 6681–6686.
  • [17] Luna-Zaragoza D, Romero-Guzmán ET, Reyes-Gutiérrez LR. Surface and Physicochemical Characterization of Phosphates Vivianite, Fe2(PO4)3 and Hydroxyapatite, Ca5(PO4)3OH. Journal of Minerals and Materials Characterization and Engineering. 2009; 8: 591–609.
  • [18] Paul A, Augustine R, Hasan A, Zahid AA, Thomas S, Agatemor C, Ghosal K. Halloysite nanotube and chitosan polymer composites: Physicochemical and drug delivery properties. Journal of Drug Delivery Science and Technology. 2022; 72: 103380.
  • [19] Cicek Ozkan, B. Cellulose and chitosan biopolymer composites reinforced with graphene and their adsorption properties for basic blue 41. Cellulose. 2022; 29: 9637–9655.
  • [20] Bhagath S, Vivek A, Krishna VV, Mittal SS, Balachandran M. Synthesis and characteristics of MMT reinforced chitosan nanocomposite. Materials Today: Proceedings. 2021; 46: 4487–4492.
  • [21] Günister E, Pestreli D, Ünlü CH, Atıcı O, Güngör N. Synthesis and characterization of chitosan-MMT biocomposite systems. Carbohydrate Polymers. 2007; 67: 358–365.
  • [22] Paluszkiewicz C, Stodolak E, Hasik M & Blazewicz, M. FT-IR study of montmorillonite–chitosan nanocomposite materials. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2011; 79(4): 784-788.
  • [23] Mohammed ASY, Dyab AK, Taha F, Abd El-Mageed, A. I. Pollen-derived microcapsules for aspirin microencapsulation: in vitro release and physico-chemical studies. RSC advances. 2022; 12(34): 22139-22149.
  • [24] Ravi Sankar V, Dachinamoorthi D, Chandra Shekar KB. A Comparative Pharmacokinetic study of Aspirin Suppositories and Aspirin Nanoparticles Loaded Suppositories. Clinic Pharmacol Biopharm. 2012; 1(105): 2.
  • [25] Vyskočilová E, Luštická I, Paterová I, Machová L, Červený L. Modified MCM-41 as a drug delivery system for acetylsalicylic acid. Solid state sciences. 2014; 38: 85-89.
  • [26] Dong LE, Gou G, Jiao L. Characterization of a dextran–coated layered double hydroxide acetylsalicylic acid delivery system and its pharmacokinetics in rabbit. Acta Pharmaceutica Sinica B. 2013; 3(6): 400-407.
There are 26 citations in total.

Details

Primary Language English
Subjects Materials Science and Technologies
Journal Section Articles
Authors

Dilay Sezer 0000-0003-1537-0744

Zeynep Aktaş 0000-0002-1070-5560

Seda Hoşgün 0000-0002-5884-9723

Emir Zafer Hoşgün 0000-0002-3810-701X

Berrin Bozan 0000-0002-3112-5784

Project Number 22ADP087
Publication Date September 30, 2024
Submission Date January 31, 2024
Acceptance Date August 6, 2024
Published in Issue Year 2024 Volume: 25 Issue: 3

Cite

AMA Sezer D, Aktaş Z, Hoşgün S, Hoşgün EZ, Bozan B. EFFICIENT DRUG CARRIER FOR ACETYLSALICYLIC ACID FROM CHITOSAN-BASED COMPOSITES PREPARED WITH MONTMORILLONITE, CELLULOSE AND HYDROXYAPATITE. Estuscience - Se. September 2024;25(3):368-379. doi:10.18038/estubtda.1428785