Fast-disintegrating sublingual tablets: Effect of epinephrine load on tablet characteristics

被引:0
作者
Mutasem M. Rawas-Qalaji
F. Estelle
R. Simons
Keith J. Simons
机构
[1] University of Manitoba,Faculty of Pharmacy
[2] University of Manitoba,Section of Allergy and Clinical Immunology, Department of Pediatrics and Child Health, Faculty of Medicine
[3] University of Manitoba,Faculty of Pharmacy, Department of Pediatrics and Child Health, Faculty of Medicine
来源
AAPS PharmSciTech | / 7卷
关键词
sublingual; transmucosal drug delivery; fastdisintegrating tablets; epinephrine; anaphylaxis;
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摘要
The aim of this study was to evaluate the effect of increasing epinephrine load on the characteristics of fast-disintegrating sublingual tablets for the potential emergency treatment of anaphylaxis. Four tablet formulations, A, B, C, and D, containing 0%, 6%, 12%, and 24% of epinephrine bitartrate, respectively, and microcrystalline cellulose:low-substituted hydroxypropyl cellulose (9∶1), were prepared by direct compression, at a range of compression forces. Tablet weight variation, content uniformity, hardness, disintegration time, wetting time, and friability were measured for each formulation at each compression force. All 4 tablet formulations at each compression force were within the United States Pharmacopeia (USP) limits for weight variation and content uniformity. A linear increase in compression force resulted in an exponential increase in hardness for all formulations, a linear increase in disintegration and wetting times of A, and an exponential increase in disintegration and wetting times of B, C, and D. At a mean±SD hardness of ≥2.3±0.2 kg, all tablet formulations passed the USP friability test. At a mean±SD hardness of ≤3.1±0.2 kg, all tablet formulations resulted in disintegration and wetting times of <10 seconds and <30 seconds, respectively. Tablets with drug loads from 0% to 24% epinephrine can be formulated with hardness, disintegration times, and wetting times suitable for sublingual administration.
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[1]  
Birudaraj R(2005)Buccal permeation of buspirone: mechanistic studies on transport pathways J Pharm Sci 94 70-78
[2]  
Berner B(2001)Pharmacokinetics of acetaminophen from rapidly disintegrating compressed tablet prepared using microcrystalline cellulose (PH-M-06) and spherical sugar granules Chem Pharm Bull (Tokyo) 49 230-232
[3]  
Shen S(1997)Single-dose pharmacokinetics of sublingual versus oral administration of micronized 17 beta-estradiol Obstet Gynecol 89 340-345
[4]  
Li X(2005)The diagnosis and management of anaphylaxis: an updated practice parameter J Allergy Clin Immunol 115 483-S523
[5]  
Ishikawa T(2003)Use of epinephrine in the treatment of anaphylaxis Curr Opin Allergy Clin Immunol 3 313-318
[6]  
Koizumi N(2006)First-aid treatment of anaphylaxis to food: focus on epinephrine J Allergy Clin Immunol 113 837-844
[7]  
Mukai B(2006)Sublingual epinephrine administration in humans: a preliminary study J Allergy Clin Immunol 113 260-260
[8]  
Price TM(2006)Sublingual epinephrine tablets versus intramuscular injection of epinephrine: Dose equivalence for potential treatment of anaphylaxis J Allergy Clin Immunol 117 398-403
[9]  
Blauer KL(2003)Rapid-dissolve technology: an interview with Loyd V. Allen Int J Pharm Technol 7 449-450
[10]  
Hansen M(2006)Orally fast disintegrating tablets: developments, technologies, taste-making and clinical studies Crit Rev Ther Drug Carrier Syst 21 433-476