Literature DB >> 21102402

OROS® hydromorphone in chronic pain management: when drug delivery technology matches clinical needs.

F Coluzzi1, C Mattia.   

Abstract

The osmotic-controlled release oral delivery system (OROS®) is an innovative drug delivery technology that uses osmotic pressure as the driving force to deliver pharmacotherapies in many therapeutic areas. In chronic pain management requiring long-term therapy, pharmaceutical technologies that ensure the controlled release of analgesic medications are imperative. In addition, once-daily formulations ensure better patient compliance to prescribed therapies. Hydromorphone was the first opioid to be formulated as a once-daily preparation using OROS® technology. The purpose of this review is to discuss the application of OROS® technology in the field of chronic pain management and to examine clinical trial results for OROS® Hydromorphone. OROS® hydromorphone ensures the constant delivery of hydromorphone over a 24-hour period, and its pharmacokinetic profile is only minimally affected by food and alcohol. Dose-conversion studies have shown that patients with chronic pain can be easily switched from previous opioid therapies to OROS® hydromorphone without a loss of pain control. These studies support the clinical utility of the 5:1 ratio used for the conversion of oral morphine to oral OROS® hydromorphone. Furthermore, once-daily OROS® hydromorphone has been shown to be effective in patients with chronic cancer and non-cancer pain, and it provides similar pain relief to SR morphine and ER oxycodone. In chronic pain management, OROS® products can result in more stable drug concentrations, reduced dosing frequency and an improved safety profile.

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Year:  2010        PMID: 21102402

Source DB:  PubMed          Journal:  Minerva Anestesiol        ISSN: 0375-9393            Impact factor:   3.051


  7 in total

1.  A prospective, open-label, multicenter study of the clinical efficacy of extended-release hydromorphone in treating cancer pain inadequately controlled by other analgesics.

Authors:  Hye-Suk Han; Ki Hyeong Lee; Kyung Hee Lee; Jeong Seon Ryu; Young Chul Kim; Seung Woo Park; Ho-Suk Oh; Kyung Tae Park; Jung Hye Kwon; Pyung Bok Lee; Won Sik Lee; Yang Soo Kim; Joong Bae Ahn; Seong Woo Jeon; Sung Yong Lee; Young Mi Seol; Jung Hun Kang; Young Jin Yuh; So Yeon Oh; Suk Ran Kim; Jin Seok Ahn
Journal:  Support Care Cancer       Date:  2013-11-08       Impact factor: 3.603

2.  Opioid Rotation in Cancer Pain Treatment.

Authors:  Michael Schuster; Oliver Bayer; Florian Heid; Rita Laufenberg-Feldmann
Journal:  Dtsch Arztebl Int       Date:  2018-03-02       Impact factor: 5.594

3.  Gastrointestinal-resident, shape-changing microdevices extend drug release in vivo.

Authors:  Arijit Ghosh; Ling Li; Liyi Xu; Ranjeet P Dash; Neha Gupta; Jenny Lam; Qianru Jin; Venkata Akshintala; Gayatri Pahapale; Wangqu Liu; Anjishnu Sarkar; Rana Rais; David H Gracias; Florin M Selaru
Journal:  Sci Adv       Date:  2020-10-28       Impact factor: 14.136

Review 4.  Assessing and Treating Chronic Pain in Patients with End-Stage Renal Disease.

Authors:  Flaminia Coluzzi
Journal:  Drugs       Date:  2018-09       Impact factor: 9.546

5.  Design and in vivo evaluation of oxycodone once-a-day controlled-release tablets.

Authors:  Ju-Young Kim; Sung-Hoon Lee; Chun-Woong Park; Yun-Seok Rhee; Dong-Wook Kim; Junsang Park; Moonseok Lee; Jeong-Woong Seo; Eun-Seok Park
Journal:  Drug Des Devel Ther       Date:  2015-01-30       Impact factor: 4.162

6.  Spatiotemporal quantification of local drug delivery using MRI.

Authors:  Morgan B Giers; Alex C McLaren; Jonathan D Plasencia; David Frakes; Ryan McLemore; Michael R Caplan
Journal:  Comput Math Methods Med       Date:  2013-04-24       Impact factor: 2.238

Review 7.  Testosterone deficiency in non-cancer opioid-treated patients.

Authors:  F Coluzzi; D Billeci; M Maggi; G Corona
Journal:  J Endocrinol Invest       Date:  2018-10-20       Impact factor: 4.256

  7 in total

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