Development of mucoadhesive microbeads using thiolated sodium alginate for intrapocket delivery of resveratrol

被引:32
|
作者
Kassem, Abeer Ahmed [1 ,2 ]
Farid, Ragwa Mohamed [3 ]
Issa, Doaa Ahmed Elsayed [4 ,5 ]
Khalil, Doaa Said [6 ]
Abd-El-Razzak, Mona Yehia [7 ]
Saudi, Hussein Ibrahim [7 ]
Eltokhey, Heba Mohamed [8 ]
El-zamarany, Enas Arafa [9 ]
机构
[1] Princess Nourah bint Abdulrahman Univ, Dept Pharmaceut Sci, Fac Pharm, Riyadh, Saudi Arabia
[2] Univ Alexandria, Fac Pharm, Dept Pharmaceut, Alexandria, Egypt
[3] Pharos Univ Alexandria, Fac Pharm & Drug Mfg, Dept Pharmaceut, Alexandria, Egypt
[4] Beirut Arab Univ, Fac Pharm, Dept Pharmaceut Sci, Beirut, Lebanon
[5] Univ Alexandria, Fac Pharm, Dept Pharmaceut Chem, Alexandria, Egypt
[6] Pharos Univ Alexandria, Fac Dent, Dept Oral Med Periodontol Oral Diag & Radiol, Alexandria, Egypt
[7] Tanta Univ, Dept Oral Med Periodontol Oral Diag & Radiol, Fac Dent, Tanta, Egypt
[8] Tanta Univ, Fac Dent, Dept Oral Biol, Tanta, Egypt
[9] Tanta Univ, Fac Med, Dept Clin Pathol, Tanta, Egypt
关键词
Polyphenol; Ionotropic gelation; Alginate - thioglycolic acid conjugate; Periodontal; DRUG-RELEASE; IN-VITRO; SYSTEMS; POLYMERS; BEADS; CONJUGATE; THIOMERS; CYSTEINE; DESIGN;
D O I
10.1016/j.ijpharm.2015.04.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Resveratrol (Res), a polyphenolic phytoalexin, had shown a promising therapeutic efficacy towards treatment of periodontal disease in vitro. This work aims to develop Res microbeads with strong mucoadhesion using thiolated alginate (TA) for local treatment of periodontal pockets. TA was synthesized by conjugating sodium alginate (A) with thioglycolic acid. Product was evaluated by IR and DSC. Both A and A: TA Res microbeads with different ratios were prepared by ionotropic gelation method. Formulations were evaluated regarding their entrapment efficiency (%EE), swelling index (SI), in vitro drug release and kinetics. Selected formula was examined for its mucoadhesion by ex vivo wash-off method, surface morphology using scanning electron microscope (SEM) and stability against light. Clinical evaluation is running. Formation of TA was confirmed. % EE for all formulations ranged from 83.72 to 104.54%. Results revealed a significant lower SI for TA rich formulation (A/TA 1: 1) along with slower release rate and zero-order kinetics, in addition to powerful mucoadhesion; 26% remaining of microbeads after 1 h, compared to 2% for A microbeads. SEM micrographs showed a rough surface with drug precipitation. The formula maintained its % EE after 5 h exposure to direct sunlight. A/TA 1: 1 mucoadhesive Res microbeads could be exploited as a prolonged drug release devices for intrapocket application. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:305 / 313
页数:9
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