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Novel modified nanoporous silica for oral drug delivery: loading and release of clarithromycin
Authors:Iman?Jabbari Zahir Abadi,Omid?Sadeghi,Hamid?Reza?Lotfizadeh Zhad,Najmeh?Tavassoli,Vahid?Amani,Mostafa?M.?Amini  author-information"  >  author-information__contact u-icon-before"  >  mailto:m-pouramini@cc.sbu.ac.ir"   title="  m-pouramini@cc.sbu.ac.ir"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Department of Pharmacology and Toxicology, Tehran Medical Unit, Islamic Azad University, P.O. Box 141556153, Tehran, Iran;(2) Department of Chemistry, Islamic Azad University, Shahr-e-Rey Branch, P.O. Box 18155-144, Tehran, Iran;(3) Department of Chemistry, Faculty of Science, Shahid Beheshti University, 1983963113, G. C. Tehran, Iran;
Abstract:Nanoporous silica SBA-15 was prepared to evaluate its application as an oral drug delivery system. A series of surface-functionalized nanopore materials as efficient clarithromycin delivery carriers was investigated. An efficient pH-responsive carrier system was constructed by hydrogen bond interaction between carboxyl and hydroxyl groups in the clarithromycin and the amine group in modified SBA-15. HPLC analyses of clarithromycin were run on a C18 column using a mobile phase comprised of potassium dihydrogen phosphate, acetonitrile and methanol (30:40:30, v/v/v). Active molecules such as clarithromycin could be stored and released from the pore voids of SBA-15 by changing the pH. The amount of clarithromycin stored in the pores of nanoporous silica based on TREN [tris(2-aminoethyl) amine]-modified SBA-15 rods was up to 46 ± 4.8 wt% at pH 8. In addition, when the pH was below 4, clarithromycin was steadily released from the pores of SBA-15 (up to 97 wt% in simulated gastric medium).
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