Turkish Journal of Bioethics. 2016; 13(1): 1-9 | DOI: 10.5505/tjps.2016.03511  

Formulatýon and In Vitro Evaluation of Modified Pulsincap of Amlodipine Besylate: An Improved Approach for the Treatment of Hypertension

Sharmin Jahan Chisty, Sumaiya Mehjabin Tosha, Ashima Aziz, Mohiuddin Ahmed Bhuiyan
Pharmaceutical Technology Research Laboratory, Department Of Pharmacy,university Of Asia Pacific, House-73, Road-5a, Dhanmondi, Dhaka-1209, Bangladesh

Pulsatile system is gaining a lot of interest as it increases patient compliance by means of providing time and site specific drug delivery system. The aim of the present study was to formulate and evaluate pulsatile drug delivery system of amlodipine besylate based on chronopharmaceutical approach for the treatment of hypertension. The basic design involves the preparation of cross-linked hard gelatin capsules by using formaldehyde. Due to formaldehyde treatment the length, external diameter, thickness, weight of the capsules was increased. Then the drug diluents mixture were prepared and loaded in, which was separated by using hydrogel plugs such as HPMC 50 cP, 100 cP, K100LV, methocel K15, sodium CMC, carbopol 971 and xanthan gum at different amount. Prepared formulations were subjected to in vitro drug release studies. From the in vitro dissolution studies it was found that by increasing the amount of polymer, release rate was decreased. The release rate was above 90% when we used 50 mg and 75 mg polymer (in each hydrogel plug), but in case of using 100 mg polymer the release rate was 70% to 85% in 10 hr. That means, in 12 hr these formulations can give a satisfactory result which is the most desire in pulsatile drug delivery system. Furthermore, the release data of all formulations were fitted to various mathematical models such as zero order, first order, Korsmeyer Peppas, Higuchi and Hixson-Crowell kinetics. The drug release follows mixed order kinetics and mechanism was found to be non-Fickian diffusion. From the result it was concluded that, all formulations showed compliance with chronotherapeutic objective of hypertension and these modified pulsincap formulations can be a best alternative for high blood pressure patient to avoid multiple dosing. However, further studies can be performed to determine the accurate dosing and better therapeutic effect.

Keywords: Pulsatile drug delivery, amlodipine besylate, cross-linked hard gelatin capsule, hydrogel plug


Formulatýon and In Vitro Evaluation of Modified Pulsincap of Amlodipine Besylate: An Improved Approach for the Treatment of Hypertension

Sharmin Jahan Chisty, Sumaiya Mehjabin Tosha, Ashima Aziz, Mohiuddin Ahmed Bhuiyan
Pharmaceutical Technology Research Laboratory, Department Of Pharmacy,university Of Asia Pacific, House-73, Road-5a, Dhanmondi, Dhaka-1209, Bangladesh

Pulsatile system is gaining a lot of interest as it increases patient compliance by means of providing time and site specific drug delivery system. The aim of the present study was to formulate and evaluate pulsatile drug delivery system of amlodipine besylate based on chronopharmaceutical approach for the treatment of hypertension. The basic design involves the preparation of cross-linked hard gelatin capsules by using formaldehyde. Due to formaldehyde treatment the length, external diameter, thickness, weight of the capsules was increased. Then the drug diluents mixture were prepared and loaded in, which was separated by using hydrogel plugs such as HPMC 50 cP, 100 cP, K100LV, methocel K15, sodium CMC, carbopol 971 and xanthan gum at different amount. Prepared formulations were subjected to in vitro drug release studies. From the in vitro dissolution studies it was found that by increasing the amount of polymer, release rate was decreased. The release rate was above 90% when we used 50 mg and 75 mg polymer (in each hydrogel plug), but in case of using 100 mg polymer the release rate was 70% to 85% in 10 hr. That means, in 12 hr these formulations can give a satisfactory result which is the most desire in pulsatile drug delivery system. Furthermore, the release data of all formulations were fitted to various mathematical models such as zero order, first order, Korsmeyer Peppas, Higuchi and Hixson-Crowell kinetics. The drug release follows mixed order kinetics and mechanism was found to be non-Fickian diffusion. From the result it was concluded that, all formulations showed compliance with chronotherapeutic objective of hypertension and these modified pulsincap formulations can be a best alternative for high blood pressure patient to avoid multiple dosing. However, further studies can be performed to determine the accurate dosing and better therapeutic effect.

Anahtar Kelimeler: Pulsatile drug delivery, amlodipine besylate, cross-linked hard gelatin capsule, hydrogel plug


Sharmin Jahan Chisty, Sumaiya Mehjabin Tosha, Ashima Aziz, Mohiuddin Ahmed Bhuiyan. Formulatýon and In Vitro Evaluation of Modified Pulsincap of Amlodipine Besylate: An Improved Approach for the Treatment of Hypertension. Turkish Journal of Bioethics. 2016; 13(1): 1-9

Corresponding Author: Mohiuddin Ahmed Bhuiyan, Bangladesh


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