Development of Metronidazole Loaded Chitosan Nanoparticles Using QbD Approach-A Novel and Potential Antibacterial Formulation

被引:38
作者
Sreeharsha, Nagaraja [1 ,2 ]
Rajpoot, Kuldeep [3 ]
Tekade, Muktika [4 ]
Kalyane, Dnyaneshwar [5 ]
Nair, Anroop B. [1 ]
Venugopala, Katharigatta N. [1 ,6 ]
Tekade, Rakesh K. [5 ,7 ,8 ]
机构
[1] King Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, Al Hasa 31982, Saudi Arabia
[2] Vidya Siri Coll Pharm, Dept Pharmaceut, Sarjapura Rd, Bangalore 560035, Karnataka, India
[3] Guru Ghasidas Vishwavidyalaya, Inst Pharmaceut Sci, Pharmaceut Res Project Lab, Bilaspur 495009, India
[4] TIT Coll Pharm, Technocrats Inst Technol Campus,Raisen Rd, Bhopal 462021, India
[5] Natl Inst Pharmaceut Educ & Res NIPER Ahmedabad, Opposite Air Force Stn Palaj, Gandhinagar 382355, India
[6] Durban Univ Technol, Dept Biotechnol & Food Technol, ZA-4001 Durban, South Africa
[7] Int Med Univ, Sch Pharm, Dept Pharmaceut Technol, Kuala Lumpur 57000, Malaysia
[8] Indian Inst Technol Jammu, Dept Mat Engn, PO Nagrota, Jammu 181221, India
关键词
metronidazole; nanoparticles; chitosan; QbD; Eudragit S100; colon-specific delivery;
D O I
10.3390/pharmaceutics12100920
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to design, optimize, and develop metronidazole (Met) loaded nanoparticles (MetNp) by employing quality-based design (QbD) as well as a risk assessment methodology. A fractional factorial design was used by selecting five independent variables viz., chitosan concentration, tripolyphosphate concentration, and acetic acid concentration as material attributes, stirring speed, and stirring time as process parameters, whereby their influence on two dependent variables such as particle size (PS) and %entrapment efficiency (%EE) was studied. MetNp were synthesized by employing an ionic-gelation technique and optimized formula obtained from the QbD design study. PS and %EE studies revealed the formation of MetNp with 558.06 +/- 2.52 nm and 59.07 +/- 2.15%, respectively. Furthermore, a Met release study in various simulated gastro-intestinal media suggested pH-triggered (pH > 7.0) and sustained release profile of Met from Eudragit S100 enteric-coated MetNp capsule (MetNp cap). Moreover, the stability investigation of formulations confirmed good stability with respect to their PS and residual drug content (RDC) at different temperature conditions. In conclusion, the QbD method was effectively utilized in the development of MetNp and enteric-coated MetNp cap depicting their potential to release Met through MetNp cap only in the colon region and can be utilized for the treatment of amoebiasis in the colon.
引用
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页码:1 / 22
页数:22
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