Abstract
Purpose: To develop and determine the in vivo performance of a capsule-based pulsatile drug delivery system containing salbutamol sulphate Methods: A controlled pulsatile release of drug after a programmed 4 h lag period was achieved from cross-linked gelatin capsule shells containing salbutamol pellets, and sealed with a suitable mixture of sodium alginate and ethyl cellulose as plug. In order to confirm the utility of developed system for the management of nocturnal asthma, a crossover study was conducted. six male rabbits were fasted overnight and divided into two groups comprised of 3 rabbits each. The individual rabbits were administered the developed pulsatile capsule and immediate release salbutamol capsule as reference,seeparately. Blood samples were collected from the ear vein of the animals into heparinized tubes and used to determine pharmacokinetic parameters, namely, maximum plasma concentration (Cmax), time to reach maximum plasma concentration (Tmax), and area under the plasma concentration - time curve (AUC0-‡) using a validated HPLC method.Results: It was observed that drug release from the optimized time-controlled capsule stopped for a period of approximately 4.25 h with an average Cmax and Tmax of 271.54 } 58.95 ng/ml and 6.00 } 0.25h. The AUC0-‡ of salbutamol after administration of the time-controlled pulsatile system was 2494.73 } 525.95 ng h/ml while that of the immediate-release formulation was 2352.77 } 432.51 ng h/ml. UsingANOVA at a significant difference of p < 0.05 (CI 95%), there was no significant difference for the AUC0-‡ between immediate release and the pulsatile capsule developed.Conclusion: The developed system is capable of releasing salbutamol after a 4 h lag period and can be considered as promising delivery system for time-controlled (pulsatile) delivery of the medication for the management of nocturnal asthma.Keywords: pH-controlled release, Lag time, Pulsatile release, Hydrocolloid plug, Nocturnal asthma.
Highlights
Up till the early 1990s, efforts were mainly to design drug delivery systems which will release the drug at fairly constant rate
Disintegrating pellets with good flow properties, smooth surface, a narrow particle size distribution and optimum elasticity and plasticity of the mass were obtained by combining Avicel PH 101 and lactose in the ratio of 70:20, together with 5 % drug, 3 % AcDiSol, and 2 % PVP K30
A total of 4 h lag time was intended for this pulsatile capsule
Summary
Up till the early 1990s, efforts were mainly to design drug delivery systems which will release the drug at fairly constant rate. These systems turned to be one of the most successful systems in delivering the drug molecule [1]. Still for many of the drugs, use of such systems is not suitable because of a number of reasons This is true in cases where the drug is subjected to large metabolic degradation. Drugs which exhibit tolerance should not be delivered at a constant rate, since the drug effect decreases with time at constant drug level In such cases it is preferable to opt for a dosage form which will provide concentration of drug at particular time point only [2]
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