Literature DB >> 12908851

Drug delivery systems for treatment of systemic hypertension.

L Michael Prisant1, William J Elliott.   

Abstract

Novel drug delivery systems are available in many areas of medicine. Their application in the treatment of hypertension continues to widen. Oral drug delivery systems permit antihypertensive agents that were previously administered two to four times daily to be administered once daily. Biotechnical use of chemical-dispensing systems has been applied to propranolol (polymer coated beads), clonidine (transdermal therapeutic system), nifedipine (osmotic pump and coat-core), isradipine (osmotic pump), verapamil (sodium alginate and spheroidal oral delivery absorption system), felodipine (coat-core), nisoldipine (coat-core) and diltiazem (polymer coated beads and Geomatrix. The initial goal was to lower blood pressure by a uniform amount throughout the entire day. Now, new drug delivery systems are being developed to target blood pressure in the early morning hours when most cardiovascular events occur. Two chronotherapeutic drug delivery systems are now available for verapamil (chronotherapeutic oral delivery absorption system and delayed coat osmotic pump). Disadvantages of sustained-release products include delayed achievement of pharmacodynamic effect, unpredictable bioavailability, enhanced first-pass hepatic metabolism, dose dumping, sustained toxicity, dosage inflexibility and increased cost. Potential advantages include reduced administration frequency, enhanced adherence and convenience, reduced toxicity, stable drug concentrations, uniform drug effect, decreased cost (occasionally) and decreased daily dosage.

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Year:  2003        PMID: 12908851     DOI: 10.2165/00003088-200342110-00001

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  51 in total

1.  A steady-state evaluation of the bioavailability of chronotherapeutic oral drug absorption system verapamil PM after nighttime dosing versus immediate-acting verapamil dosed every eight hours.

Authors:  L M Prisant; J G Devane; J Butler
Journal:  Am J Ther       Date:  2000-11       Impact factor: 2.688

2.  Effects of doxazosin in the gastrointestinal therapeutic system formulation versus doxazosin standard and placebo in mild-to-moderate hypertension. Doxazosin Investigators' Study Group.

Authors:  I Os; H P Stokke
Journal:  J Cardiovasc Pharmacol       Date:  1999-05       Impact factor: 3.105

3.  Impact of food on the pharmacokinetics and electrocardiographic effects of sustained release verapamil in normal subjects.

Authors:  T J Hoon; P L McCollam; K J Beckman; R J Hariman; J L Bauman
Journal:  Am J Cardiol       Date:  1992-10-15       Impact factor: 2.778

4.  Clinical pharmacokinetics of doxazosin in a controlled-release gastrointestinal therapeutic system (GITS) formulation.

Authors:  M Chung; V Vashi; J Puente; M Sweeney; P Meredith
Journal:  Br J Clin Pharmacol       Date:  1999-11       Impact factor: 4.335

5.  Doxazosin GITS compared with doxazosin standard and placebo in patients with mild hypertension.

Authors:  I Os; H P Stokke
Journal:  Blood Press       Date:  1999       Impact factor: 2.835

6.  Securon SR: sustained-release verapamil.

Authors: 
Journal:  Drug Ther Bull       Date:  1987-06-15

7.  Hypertension and chronotherapy: shifting the treatment paradigm.

Authors:  L M Prisant
Journal:  Am J Hypertens       Date:  2001-09       Impact factor: 2.689

Review 8.  Verapamil revisited: a transition in novel drug delivery systems and outcomes.

Authors:  L M Prisant
Journal:  Heart Dis       Date:  2001 Jan-Feb

9.  Improved compliance measures: applications in an ambulatory hypertensive drug trial.

Authors:  P Rudd; S Ahmed; V Zachary; C Barton; D Bonduelle
Journal:  Clin Pharmacol Ther       Date:  1990-12       Impact factor: 6.875

10.  Design of a new multiple-unit controlled-release formulation of metoprolol--metoprolol CR.

Authors:  A Sandberg; G Ragnarsson; U E Jonsson; J Sjögren
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

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  5 in total

1.  Antihypertensive pharmacobezoar.

Authors:  L Michael Prisant; Vernon C Spaulding
Journal:  J Clin Hypertens (Greenwich)       Date:  2006-04       Impact factor: 3.738

Review 2.  Nanotechnology Based Approaches for Enhancing Oral Bioavailability of Poorly Water Soluble Antihypertensive Drugs.

Authors:  Mayank Sharma; Rajesh Sharma; Dinesh Kumar Jain
Journal:  Scientifica (Cairo)       Date:  2016-04-30

3.  High-Throughput Excipient Discovery Enables Oral Delivery of Poorly Soluble Pharmaceuticals.

Authors:  Jeffrey M Ting; Swapnil Tale; Anatolii A Purchel; Seamus D Jones; Lakmini Widanapathirana; Zachary P Tolstyka; Li Guo; Steven J Guillaudeu; Frank S Bates; Theresa M Reineke
Journal:  ACS Cent Sci       Date:  2016-10-12       Impact factor: 14.553

Review 4.  Calcium channel blocker class heterogeneity: select aspects of pharmacokinetics and pharmacodynamics.

Authors:  Domenic A Sica
Journal:  J Clin Hypertens (Greenwich)       Date:  2005-04       Impact factor: 3.738

5.  Association between Total Daily Doses with duration of hospitalization among readmitted patients in a multi-ethnic Asian population.

Authors:  Vivien Teo; Ming Ren Toh; Yu Heng Kwan; Sreemanee Raaj; Su-Yin Doreen Tan; Joyce Zhen Yin Tan
Journal:  Saudi Pharm J       Date:  2015-01-10       Impact factor: 4.330

  5 in total

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