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Modulation of microenvironmental pH for dual release and reduced in vivo gastrointestinal bleeding of aceclofenac using hydroxypropyl methylcellulose-based bilayered matrix tablet.
Eur J Pharm Sci. 2017 May 01; 102:85-93.EJ

Abstract

This study was designed to develop a once-daily controlled-release matrix tablet of aceclofenac 200mg (AFC-CR) with dual release characteristics and to investigate the role of an alkalizer in enhancing drug solubility and reducing the occurrence of gastroduodenal mucosal lesions. Two formulation approaches were employed, namely a monolithic matrix tablet and a bilayered tablet. In vitro dissolution studies of AFC-CR tablets were carried out in simulated intestinal fluid (pH6.8 buffer). The in vivo pharmacokinetic studies and drug safety of the immediate-release reference tablet Airtal® 100mg (Daewoong Co., Korea) and the optimized AFC-CR tablet were compared in beagle dogs under fasted condition. The optimally selected AFC-CR formulation displayed the desired dual release characteristics in simulated intestinal fluid with satisfactory micromeritic properties. The swelling action of the optimal matrix tablet, which was visualized by near-infrared (NIR) chemical imaging, occurred rapidly following hydration. Incorporation of sodium carbonate (Na2CO3) was found to enhance the release rate of the AFC-CR bilayered tablets at early stages and increase the microenvironmental pH (pHM). A pharmacokinetic study in beagle dogs indicated a higher drug plasma concentration and a sustained-release pattern for the AFC-CR tablet compared to the Airtal® tablet. AFC-CR was also superior to Airtal® in terms of in vivo drug safety, since no beagle dog receiving AFC-CR experienced gastrointestinal bleeding. The significant enhancement of drug safety was attributed to the size reduction and the increase of pHM of drug particles by means of incorporation of the alkalizer. These findings provide a scientific rationale for developing a novel controlled-release matrix tablet with enhanced patient compliance and better pain control.

Authors+Show Affiliations

College of Pharmacy, Ajou University, Suwon 16499, Republic of Korea; Korea United Pharm Inc., Seoul 135010, Republic of Korea.College of Pharmacy, Ajou University, Suwon 16499, Republic of Korea.College of Pharmacy, Ajou University, Suwon 16499, Republic of Korea.Korea United Pharm Inc., Seoul 135010, Republic of Korea.College of Pharmacy, Ajou University, Suwon 16499, Republic of Korea; Institute of Pharmaceutical Science and Technology, Ajou University, Suwon 16499, Republic of Korea. Electronic address: bjl@ajou.ac.kr.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28263912

Citation

Kang, Won-Ho, et al. "Modulation of Microenvironmental pH for Dual Release and Reduced in Vivo Gastrointestinal Bleeding of Aceclofenac Using Hydroxypropyl Methylcellulose-based Bilayered Matrix Tablet." European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences, vol. 102, 2017, pp. 85-93.
Kang WH, Nguyen HV, Park C, et al. Modulation of microenvironmental pH for dual release and reduced in vivo gastrointestinal bleeding of aceclofenac using hydroxypropyl methylcellulose-based bilayered matrix tablet. Eur J Pharm Sci. 2017;102:85-93.
Kang, W. H., Nguyen, H. V., Park, C., Choi, Y. W., & Lee, B. J. (2017). Modulation of microenvironmental pH for dual release and reduced in vivo gastrointestinal bleeding of aceclofenac using hydroxypropyl methylcellulose-based bilayered matrix tablet. European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences, 102, 85-93. https://doi.org/10.1016/j.ejps.2017.02.039
Kang WH, et al. Modulation of Microenvironmental pH for Dual Release and Reduced in Vivo Gastrointestinal Bleeding of Aceclofenac Using Hydroxypropyl Methylcellulose-based Bilayered Matrix Tablet. Eur J Pharm Sci. 2017 May 1;102:85-93. PubMed PMID: 28263912.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Modulation of microenvironmental pH for dual release and reduced in vivo gastrointestinal bleeding of aceclofenac using hydroxypropyl methylcellulose-based bilayered matrix tablet. AU - Kang,Won-Ho, AU - Nguyen,Hien Van, AU - Park,Chulhun, AU - Choi,Youn-Woong, AU - Lee,Beom-Jin, Y1 - 2017/03/02/ PY - 2016/10/23/received PY - 2017/01/16/revised PY - 2017/02/27/accepted PY - 2017/3/7/pubmed PY - 2018/3/3/medline PY - 2017/3/7/entrez KW - Aceclofenac KW - Bilayered tablet KW - Dual release KW - In vivo drug safety KW - Microenvironmental pH KW - Monolithic matrix tablet SP - 85 EP - 93 JF - European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences JO - Eur J Pharm Sci VL - 102 N2 - This study was designed to develop a once-daily controlled-release matrix tablet of aceclofenac 200mg (AFC-CR) with dual release characteristics and to investigate the role of an alkalizer in enhancing drug solubility and reducing the occurrence of gastroduodenal mucosal lesions. Two formulation approaches were employed, namely a monolithic matrix tablet and a bilayered tablet. In vitro dissolution studies of AFC-CR tablets were carried out in simulated intestinal fluid (pH6.8 buffer). The in vivo pharmacokinetic studies and drug safety of the immediate-release reference tablet Airtal® 100mg (Daewoong Co., Korea) and the optimized AFC-CR tablet were compared in beagle dogs under fasted condition. The optimally selected AFC-CR formulation displayed the desired dual release characteristics in simulated intestinal fluid with satisfactory micromeritic properties. The swelling action of the optimal matrix tablet, which was visualized by near-infrared (NIR) chemical imaging, occurred rapidly following hydration. Incorporation of sodium carbonate (Na2CO3) was found to enhance the release rate of the AFC-CR bilayered tablets at early stages and increase the microenvironmental pH (pHM). A pharmacokinetic study in beagle dogs indicated a higher drug plasma concentration and a sustained-release pattern for the AFC-CR tablet compared to the Airtal® tablet. AFC-CR was also superior to Airtal® in terms of in vivo drug safety, since no beagle dog receiving AFC-CR experienced gastrointestinal bleeding. The significant enhancement of drug safety was attributed to the size reduction and the increase of pHM of drug particles by means of incorporation of the alkalizer. These findings provide a scientific rationale for developing a novel controlled-release matrix tablet with enhanced patient compliance and better pain control. SN - 1879-0720 UR - https://www.unboundmedicine.com/medline/citation/28263912/Modulation_of_microenvironmental_pH_for_dual_release_and_reduced_in_vivo_gastrointestinal_bleeding_of_aceclofenac_using_hydroxypropyl_methylcellulose_based_bilayered_matrix_tablet_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0928-0987(17)30116-1 DB - PRIME DP - Unbound Medicine ER -