Tris (2-aminoethyl) Amine Functionalized Nanoporous Silica SBA-15 as a Potential Drug Carrier for Citalopram

Author:

Dalayi Fatemeh1,Hajiaghababaei Leila1,Badiei Alireza2,Boorboor Azimi Elham2,Ganjali Mohammad Reza3,Mohammadi Ziarani Ghodsi4

Affiliation:

1. Department of Chemistry, Yadegar-e-Imam Khomeini (RAH) Shahre Rey Branch, Islamic Azad University, Tehran, Iran

2. School of Chemistry, College of Science, University of Tehran, Tehran, Iran

3. Center of Excellence in Electrochemistry, School of Chemistry, College of Science, University of Tehran, Tehran, Iran

4. Department of Chemistry, Alzahra University, Tehran, Iran

Abstract

Introduction: Ordered nanoporous silica such as SBA-15 has a great potential for application in controlled drug release systems. Chemical modification of the silanol groups of SBA-15 allows better control over drug loading and release. Therefore, tris(2-aminoethyl) amine-functionalized mesoporous silica SBA-15 was evaluated as a potential carrier for the delivery of citalopram. Methods: Tris (2-aminoethyl) amine-functionalized SBA-15 was synthesized and characterized by various methods. Citalopram was loaded on the functionalized SBA-15 and drug release into simulated body fluid (SBF) solution and phosphate buffers was investigated. Results: The optimal condition for loading of the citalopram was obtained at pH = 9 after stirring for 5 minutes. The release profile of citalopram was monitored in phosphate buffers with three different pH values of 5, 7, and 8. A faster release rate at lower pH value was observed, suggesting a weaker interaction because of the protonation of the amino group of the functionalized SBA15. The average release rate of citalopram from each gram of functionalized SBA-15 was 12 µg h-1 in the SBF. Conclusion: The results showed that loading amount and release rate of citalopram depended on pH value and the release process showed a very slow release pattern. Therefore, tris (2-aminoethyl) amine-functionalized SBA-15 is a suitable carrier for controlled release of citalopram and has a great potential for disease therapy.

Publisher

Maad Rayan Publishing Company

Subject

General Medicine

Reference39 articles.

1. Effects of chronic treatment with citalopram on cannabinoid and opioid receptor-mediated G-protein coupling in discrete rat brain regions

2. Celexa (citalopram hydrobromide) Tablets/Oral Solution. Prescribing Information. Forest Laboratories, Inc. https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/020822s043lbl.pdf.

3. Nemeroff CB. Management of Treatment-Resistant Major Psychiatric Disorders. New York: Oxford University Press; 2012.

4. Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych (Office for Registration of Medicinal Products, Medical Devices and Biocides). http://www.urpl.gov.pl/system/drugs/dcp/charakterystyka/2012-07-02_2012-04-20-spc-citalopramvb-pl.pdf.

5. British National Formulary: BNF 76. 76th ed. Pharmaceutical Press; 2018.

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