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Formulation, in vitro evaluation and study of variables on tri-layered gastro-retentive delivery system of diltiazem HCl.
Drug Dev Ind Pharm. 2014 Mar; 40(3):380-9.DD

Abstract

CONTEXT

Tri-layered floating tablets using only one grade of polyethylene oxide (PEO) would enable easy manufacturing, reproducibility and controlled release for highly soluble drugs.

OBJECTIVE

To evaluate the potential of PEO as a sole polymer for the controlled release and to study the effect of formulation variables on release and gastric retention of highly soluble Diltiazem hydrochloride (DTZ).

METHODS

Tablets were compressed with middle layer consisting of drug and polymer while outer layers consisted of polymer with sodium bicarbonate. Design of formulation to obtain 12 h, zero-order release and rapid floatation was done by varying the grades, quantity of PEO and sodium bicarbonate. Dissolution data were fitted in drug release models and swelling/erosion studies were undertaken to verify the drug release mechanism. Effect of formulation variables and tablet surface morphology using scanning electron microscopy were studied.

RESULTS AND DISCUSSION

The optimized formula passed the criteria of USP dissolution test I and exhibited floating lag-time of 3-4 min. Drug release was faster from low molecular weight (MW) PEO as compared to high MW. With an increase in the amount of sodium bicarbonate, faster buoyancy was achieved due to the increased CO2 gas formation. Drug release followed zero-order and gave a good fit to the Korsmeyer-Peppas model, which suggested that drug release was due to diffusion through polymer swelling.

CONCLUSION

Zero-order, controlled release profile with the desired buoyancy can be achieved by using optimum formula quantities of sodium bicarbonate and polymer. The tri-layered system shows promising delivery of DTZ, and possibly other water-soluble drugs.

Authors+Show Affiliations

Massachusetts College of Pharmacy and Health Sciences (MCPHS) , Boston, MA , USA , and.No affiliation info available

Pub Type(s)

Comparative Study
Journal Article

Language

eng

PubMed ID

23369093

Citation

Raut Desai, Shilpa, and Bhagwan D. Rohera. "Formulation, in Vitro Evaluation and Study of Variables On Tri-layered Gastro-retentive Delivery System of Diltiazem HCl." Drug Development and Industrial Pharmacy, vol. 40, no. 3, 2014, pp. 380-9.
Raut Desai S, Rohera BD. Formulation, in vitro evaluation and study of variables on tri-layered gastro-retentive delivery system of diltiazem HCl. Drug Dev Ind Pharm. 2014;40(3):380-9.
Raut Desai, S., & Rohera, B. D. (2014). Formulation, in vitro evaluation and study of variables on tri-layered gastro-retentive delivery system of diltiazem HCl. Drug Development and Industrial Pharmacy, 40(3), 380-9. https://doi.org/10.3109/03639045.2012.763138
Raut Desai S, Rohera BD. Formulation, in Vitro Evaluation and Study of Variables On Tri-layered Gastro-retentive Delivery System of Diltiazem HCl. Drug Dev Ind Pharm. 2014;40(3):380-9. PubMed PMID: 23369093.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Formulation, in vitro evaluation and study of variables on tri-layered gastro-retentive delivery system of diltiazem HCl. AU - Raut Desai,Shilpa, AU - Rohera,Bhagwan D, Y1 - 2013/02/01/ PY - 2013/2/2/entrez PY - 2013/2/2/pubmed PY - 2014/10/7/medline SP - 380 EP - 9 JF - Drug development and industrial pharmacy JO - Drug Dev Ind Pharm VL - 40 IS - 3 N2 - CONTEXT: Tri-layered floating tablets using only one grade of polyethylene oxide (PEO) would enable easy manufacturing, reproducibility and controlled release for highly soluble drugs. OBJECTIVE: To evaluate the potential of PEO as a sole polymer for the controlled release and to study the effect of formulation variables on release and gastric retention of highly soluble Diltiazem hydrochloride (DTZ). METHODS: Tablets were compressed with middle layer consisting of drug and polymer while outer layers consisted of polymer with sodium bicarbonate. Design of formulation to obtain 12 h, zero-order release and rapid floatation was done by varying the grades, quantity of PEO and sodium bicarbonate. Dissolution data were fitted in drug release models and swelling/erosion studies were undertaken to verify the drug release mechanism. Effect of formulation variables and tablet surface morphology using scanning electron microscopy were studied. RESULTS AND DISCUSSION: The optimized formula passed the criteria of USP dissolution test I and exhibited floating lag-time of 3-4 min. Drug release was faster from low molecular weight (MW) PEO as compared to high MW. With an increase in the amount of sodium bicarbonate, faster buoyancy was achieved due to the increased CO2 gas formation. Drug release followed zero-order and gave a good fit to the Korsmeyer-Peppas model, which suggested that drug release was due to diffusion through polymer swelling. CONCLUSION: Zero-order, controlled release profile with the desired buoyancy can be achieved by using optimum formula quantities of sodium bicarbonate and polymer. The tri-layered system shows promising delivery of DTZ, and possibly other water-soluble drugs. SN - 1520-5762 UR - https://www.unboundmedicine.com/medline/citation/23369093/Formulation_in_vitro_evaluation_and_study_of_variables_on_tri_layered_gastro_retentive_delivery_system_of_diltiazem_HCl_ L2 - https://www.tandfonline.com/doi/full/10.3109/03639045.2012.763138 DB - PRIME DP - Unbound Medicine ER -