Clinical spectrum of the osmotic-controlled release oral delivery system (OROS), an advanced oral delivery form

被引:140
作者
Conley, Robert [1 ]
Gupta, Suneel K.
Sathyan, Gayatri
机构
[1] Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Catonsville, MD 21228 USA
[2] Alza Corp, Mountain View, CA USA
关键词
drug delivery; extended release; OROS technology; osmotic pressure; treatment compliance;
D O I
10.1185/030079906X132613
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The osmotic-controlled release oral delivery system, OROS, is an advanced drug delivery technology that uses osmotic pressure as the driving force to deliver pharmacotherapy, usually once-daily, in several therapeutic areas. Objective: The purpose of this review is to discuss the evolution of OROS technology and examine the many therapeutic areas where OROS products are being used. Methods: A search of Medline and EMBASE were performed using the keywords 'OROS' and 'osmotic delivery' for the period January 1990 to June 2005. Data were also obtained from the manufacturers' websites and associated publications. Results: OROS technology has evolved over the last 30 years, resulting in four systems: the elementary osmotic pump; the two-layer osmotic push - pull tablet; the advanced longitudinally compressed tablet multilayer formulation; and, the L-OROS system. OROS technology is employed for drug delivery in many therapeutic areas including: cardiovascular medicine, endocrinology, urology, and central nervous system ( CNS) therapeutics. Two calcium channel blockers utilizing OROS technology for the treatment of hypertension are nifedipine and verapamil. Glipizide extended-extended-release is used for the treatment of type 2 release diabetes. Doxazosin is used for the treatment of benign prostatic hyperplasia, and oxybutynin for overactive bladder. Most recent developments are with drugs that affect the CNS, including the use of methylphenidate for treatment of attention deficit hyperactivity disorder, paliperidone extended-release and OROS hydromorphone, which are under clinical development for schizophrenia and chronic pain, respectively. Conclusions: Drug delivery using the various OROS products can result in an improved safety profile, stable drug concentrations, uniform drug effects, and reduced dosing frequency. OROS technology has also enabled the use of an effective starting dose, without the need for dose titration, which allows the achievement of symptom control much earlier than that observed with immediate-release preparations. Such attributes can enhance patient compliance and convenience, thereby ensuring efficacy and improving patient outcomes.
引用
收藏
页码:1879 / 1892
页数:14
相关论文
共 89 条
[71]   The wet patient: understanding patients with overactive bladder and incontinence [J].
Serels, S .
CURRENT MEDICAL RESEARCH AND OPINION, 2004, 20 (06) :791-801
[72]   Oxybutynin extended-release - A review of its use in the management of overactive bladder [J].
Siddiqui, MAA ;
Perry, CM ;
Scott, LJ .
DRUGS, 2004, 64 (08) :885-912
[73]   Efficacy, safety, and dose-response characteristics of glipizide gastrointestinal therapeutic system on glycemic control and insulin secretion in NIDDM - Results of two multicenter, randomized, placebo-controlled clinical trials [J].
Simonson, DC ;
Kourides, IA ;
Feinglos, M ;
Shamoon, H ;
Fischette, CT ;
Aronoff, S ;
Blonde, L ;
Cefalu, W ;
Clement, S ;
Greenberg, C ;
Levin, S ;
Lucas, CP ;
Macy, C ;
Manning, J ;
Marbury, TC ;
McAdams, MJ ;
Mezitis, NHE ;
Miller, S ;
Owens, D ;
Sandler, J ;
Schwartz, SL ;
Shamoon, H ;
Sosenko, J .
DIABETES CARE, 1997, 20 (04) :597-606
[74]   Compliance with stimulants for attention-deficit/hyperactivity disorder - Issues and approaches for improvement [J].
Swanson, J .
CNS DRUGS, 2003, 17 (02) :117-131
[75]   A comparison of once-daily extended-release methylphenidate formulations in children with attention-deficit/hyperactivity disorder in the laboratory school (The COMACS study) [J].
Swanson, JM ;
Wigal, SB ;
Wigal, T ;
Sonuga-Barke, EJS ;
Greenhill, LL ;
Biederman, J ;
Kollins, S ;
Nguyen, AS ;
DeCory, HH ;
Dirksen, SJH ;
Hatch, SJ .
PEDIATRICS, 2004, 113 (03) :E206-E216
[76]   ELEMENTARY OSMOTIC PUMP [J].
THEEUWES, F .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1975, 64 (12) :1987-1991
[77]   PHARMACOKINETICS AND BIOAVAILABILITY OF HYDROMORPHONE FOLLOWING INTRAVENOUS AND ORAL-ADMINISTRATION TO HUMAN-SUBJECTS [J].
VALLNER, JJ ;
STEWART, JT ;
KOTZAN, JA ;
KIRSTEN, EB ;
HONIGBERG, IL .
JOURNAL OF CLINICAL PHARMACOLOGY, 1981, 21 (04) :152-156
[78]  
VANZWIETEN PA, 1993, J HYPERTENS, V11, pS3, DOI 10.1097/00004872-199303001-00002
[79]   Dry mouth with conventional and controlled-release oxybutynin in urinary incontinence [J].
Versi, E ;
Appell, R ;
Mobley, D ;
Patton, W ;
Saltzstein, D .
OBSTETRICS AND GYNECOLOGY, 2000, 95 (05) :718-721
[80]   Variables that affect the clinical use and abuse of methylphenidate in the treatment of ADHD [J].
Volkow, ND ;
Swanson, JM .
AMERICAN JOURNAL OF PSYCHIATRY, 2003, 160 (11) :1909-1918