Literature DB >> 31174439

Exploiting knowledge on pharmacodynamics-pharmacokinetics for accelerated anti-leishmanial drug discovery/development.

Shyam Sundar1, Neha Agrawal2, Bhawana Singh1,3.   

Abstract

Introduction: Being on the top list of neglected tropical diseases, leishmaniasis has been marked for elimination by 2020. In the light of small armamentarium of drugs and their associated drawbacks, the understanding of pharmacodynamics and/or pharmacokinetics becomes a priority to achieve and sustain disease elimination. Areas covered: The authors have looked into pharmacological aspects of existing and emerging drugs for treatment of leishmaniasis. An in-depth understanding of pharmacodynamics and pharmacokinetics (PKPD) provides a rationale for drug designing and optimizing the treatment strategies. It forms a key to prevent drug resistance and avoid drug-associated adverse effects. The authors have compiled the researches on the PKPD of different anti-leishmanial formulations that have the potential for improved and/or effective disease intervention. Expert opinion: Understanding the pharmacological aspects of drugs forms the basis for the clinical application of novel drugs. Tailoring drug dosage and individualized treatment can avoid the adverse events and bridge gap between the in vitro models and their clinical application. An integrated approach, with pragmatic use of technological advances can improve phenotypic screening and physiochemical properties of novel drugs. Concomitantly, this can serve to improve clinical efficacies, reduce the incidence of relapse and accelerate the drug discovery/development process for leishmaniasis elimination.

Entities:  

Keywords:  Pharmacology; combination therapy; host directed therapy; nano-formulations

Mesh:

Substances:

Year:  2019        PMID: 31174439      PMCID: PMC6640127          DOI: 10.1080/17425255.2019.1629417

Source DB:  PubMed          Journal:  Expert Opin Drug Metab Toxicol        ISSN: 1742-5255            Impact factor:   4.481


  212 in total

1.  Efficacy of cryotherapy and intralesional pentostam in treatment of cutaneous leishmaniasis.

Authors:  M S Gurei; N Tatli; H Ozbilge; O Erel; A Seyrek; A Kocyigit; M Ulukanligil
Journal:  J Egypt Soc Parasitol       Date:  2000-04

Review 2.  U.S. Food and Drug Administration approval of AmBisome (liposomal amphotericin B) for treatment of visceral leishmaniasis.

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Journal:  Clin Infect Dis       Date:  1999-01       Impact factor: 9.079

3.  Safety, toxicokinetics and tissue distribution of long-term intravenous liposomal amphotericin B (AmBisome): a 91-day study in rats.

Authors:  I Bekersky; G W Boswell; R Hiles; R M Fielding; D Buell; T J Walsh
Journal:  Pharm Res       Date:  2000-12       Impact factor: 4.200

4.  Successful topical treatment of murine cutaneous leishmaniasis with a combination of paromomycin (Aminosidine) and gentamicin.

Authors:  M Grogl; B G Schuster; W Y Ellis; J D Berman
Journal:  J Parasitol       Date:  1999-04       Impact factor: 1.276

5.  Safety and toxicokinetics of intravenous liposomal amphotericin B (AmBisome) in beagle dogs.

Authors:  I Bekersky; G W Boswell; R Hiles; R M Fielding; D Buell; T J Walsh
Journal:  Pharm Res       Date:  1999-11       Impact factor: 4.200

6.  Comparison of the efficacy of free and non-ionic-surfactant vesicular formulations of paromomycin in a murine model of visceral leishmaniasis.

Authors:  D Williams; A B Mullen; A J Baillie; K C Carter
Journal:  J Pharm Pharmacol       Date:  1998-12       Impact factor: 3.765

7.  A topical nitric oxide-generating therapy for cutaneous leishmaniasis.

Authors:  R N Davidson; V Yardley; S L Croft; P Konecny; N Benjamin
Journal:  Trans R Soc Trop Med Hyg       Date:  2000 May-Jun       Impact factor: 2.184

8.  A randomised, blinded, placebo-controlled clinical trial with allopurinol in canine leishmaniosis.

Authors:  A F Koutinas; M N Saridomichelakis; M E Mylonakis; L Leontides; Z Polizopoulou; C Billinis; D Argyriadis; N Diakou; O Papadopoulos
Journal:  Vet Parasitol       Date:  2001-07-27       Impact factor: 2.738

9.  Liposomal amphotericin B for empirical therapy in patients with persistent fever and neutropenia. National Institute of Allergy and Infectious Diseases Mycoses Study Group.

Authors:  T J Walsh; R W Finberg; C Arndt; J Hiemenz; C Schwartz; D Bodensteiner; P Pappas; N Seibel; R N Greenberg; S Dummer; M Schuster; J S Holcenberg
Journal:  N Engl J Med       Date:  1999-03-11       Impact factor: 91.245

10.  A prospective randomized, comparative, open-label trial of the safety and efficacy of paromomycin (aminosidine) plus sodium stibogluconate versus sodium stibogluconate alone for the treatment of visceral leishmaniasis.

Authors:  C P Thakur; T P Kanyok; A K Pandey; G P Sinha; A E Zaniewski; H H Houlihan; P Olliaro
Journal:  Trans R Soc Trop Med Hyg       Date:  2000 Jul-Aug       Impact factor: 2.184

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