The objective of this study was to formulate and evaluate gastric floating dosage forms of hollow microspheres for controlled delivery of dextromethorphan hydrobromide (DBM). Hollow microspheres were prepared by emulsion polymerization method using natural polymer gelatin as release retardant and coating agent. Hollow microspheres were characterized by FT-IR, DSC, SEM, and micromeritic properties. FT-IR and DSC studies showed no chemical interaction between the drug and polymers. Hollow microspheres were evaluated for percentage yield, encapsulation efficiency and in vitro release studies. The obtained angle of repose, % Carr’s index, Hausner ratio, and tapped density values were within the limits indicating good flow properties. The surfac...
The non-effervescent, gastro-retentive drug delivery technology known as floating microspheres (holl...
The objective of the present study was to develop floating microspheres of Captopril in order to ach...
Oral controlled release dosage forms encounter several physiological constraints like inability to r...
The objective of this study was to formulate and evaluate gastric floating dosage forms of hollow mi...
The aim of this work was to develop natural and synthetic polymer based microspheres of Dexlansopraz...
The objective of the present study was to development, characterization and evaluation of colon spec...
In this work an attempt was made to design a gastro retentive delivery system in the form of floatin...
The main aim of this study is to develop a gastro retentive multiple unit floating drug delivery sys...
Microspheres are novel drug delivery approach to control release of pharmacologically active ingredi...
Dexrabeprazole sodium (DEX) is R (+)-isomer of rabeprazole. DEX has been used in the treatment of ga...
Recently, several technical advancements have led to the development of several novel drug delivery ...
The present study aimed to improve solubility and prolong the release duration of a poorly soluble d...
Objective: The purpose of the study was to develop the multiple unit non-effervescent gastroretentiv...
Purpose: To prepare and evaluate floating microspheres of silymarin for prolonged gastric residence...
Floating microspheres of Losartan potassium was prepared solvent evaporation method with an aim of i...
The non-effervescent, gastro-retentive drug delivery technology known as floating microspheres (holl...
The objective of the present study was to develop floating microspheres of Captopril in order to ach...
Oral controlled release dosage forms encounter several physiological constraints like inability to r...
The objective of this study was to formulate and evaluate gastric floating dosage forms of hollow mi...
The aim of this work was to develop natural and synthetic polymer based microspheres of Dexlansopraz...
The objective of the present study was to development, characterization and evaluation of colon spec...
In this work an attempt was made to design a gastro retentive delivery system in the form of floatin...
The main aim of this study is to develop a gastro retentive multiple unit floating drug delivery sys...
Microspheres are novel drug delivery approach to control release of pharmacologically active ingredi...
Dexrabeprazole sodium (DEX) is R (+)-isomer of rabeprazole. DEX has been used in the treatment of ga...
Recently, several technical advancements have led to the development of several novel drug delivery ...
The present study aimed to improve solubility and prolong the release duration of a poorly soluble d...
Objective: The purpose of the study was to develop the multiple unit non-effervescent gastroretentiv...
Purpose: To prepare and evaluate floating microspheres of silymarin for prolonged gastric residence...
Floating microspheres of Losartan potassium was prepared solvent evaporation method with an aim of i...
The non-effervescent, gastro-retentive drug delivery technology known as floating microspheres (holl...
The objective of the present study was to develop floating microspheres of Captopril in order to ach...
Oral controlled release dosage forms encounter several physiological constraints like inability to r...