Hit generation in TB drug discovery: from genome to granuloma

T Yuan, NS Sampson - Chemical reviews, 2018 - ACS Publications
Current tuberculosis (TB) drug development efforts are not sufficient to end the global TB
epidemic. Recent efforts have focused on the development of whole-cell screening assays …

Bioprospecting for antibacterial drugs: a multidisciplinary perspective on natural product source material, bioassay selection and avoidable pitfalls

TPT Cushnie, B Cushnie, J Echeverría… - Pharmaceutical …, 2020 - Springer
Bioprospecting is the exploration, extraction and screening of biological material and
sometimes indigenous knowledge to discover and develop new drugs and other products …

Comprehensive physicochemical, pharmacokinetic and activity profiling of anti-TB agents

SB Lakshminarayana, TB Huat, PC Ho… - Journal of …, 2015 - academic.oup.com
Objectives The discovery and development of TB drugs has met limited success, with two
new drugs approved over the last 40 years. Part of the difficulty resides in the lack of well …

Future perspective of diabetic animal models

S Pandey, MC Dvorakova - Endocrine, Metabolic & Immune …, 2020 - ingentaconnect.com
Objective: The need of today's research is to develop successful and reliable diabetic animal
models for understanding the disease susceptibility and pathogenesis. Enormous success …

[HTML][HTML] The ins and outs of Mycobacterium tuberculosis drug susceptibility testing

EC Böttger - Clinical microbiology and infection, 2011 - Elsevier
Drug susceptibility testing of Mycobacterium tuberculosis in the diagnostic laboratory
classifies clinical isolates as either drug-'resistant'or drug-'susceptible', on the basis of their …

Current status and opportunities for therapeutic drug monitoring in the treatment of tuberculosis

MA Zuur, MS Bolhuis, R Anthony… - Expert opinion on …, 2016 - Taylor & Francis
Introduction: Tuberculosis remains a global health problem and pharmacokinetic variability
has been postulated as one of the causes of treatment failure and acquired drug resistance …

[HTML][HTML] Pharmacokinetics and pharmacodynamics of anti-tuberculosis drugs: an evaluation of in vitro, in vivo methodologies and human studies

JWC Alffenaar, JEM de Steenwinkel… - Frontiers in …, 2022 - frontiersin.org
There has been an increased interest in pharmacokinetics and pharmacodynamics (PKPD)
of anti-tuberculosis drugs. A better understanding of the relationship between drug …

PK/PD models in antibacterial development

T Velkov, PJ Bergen, J Lora-Tamayo… - Current opinion in …, 2013 - Elsevier
Highlights•In vitro PK/PD models are less costly and resource-intensive and permit
investigations of considerable duration which may not be feasible in animals.•Mouse thigh …

A microfluidic system that replicates pharmacokinetic (PK) profiles in vitro improves prediction of in vivo efficacy in preclinical models

D Singh, SP Deosarkar, E Cadogan, V Flemington… - Plos …, 2022 - journals.plos.org
Test compounds used on in vitro model systems are conventionally delivered to cell culture
wells as fixed concentration bolus doses; however, this poorly replicates the …

Controlled pharmacokinetic anti-cancer drug concentration profiles lead to growth inhibition of colorectal cancer cells in a microfluidic device

J Komen, EY Westerbeek, RW Kolkman, J Roesthuis… - Lab on a Chip, 2020 - pubs.rsc.org
We present a microfluidic device to expose cancer cells to a dynamic, in vivo-like
concentration profile of a drug, and quantify efficacy on-chip. About 30% of cancer patients …