Preclinical Evaluation of Antimicrobial Nanodrugs - Bueno, Juan
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Translational medicine addresses the gap between research and the clinical application of new discoveries. To efficiently deliver new drugs to care centers, a preclinical evaluation, both in vitro and in vivo, is required to ensure that the most active and least toxic compounds are selected as well as to predict clinical outcome.
Antimicrobial nanomedicines have been shown to have higher specificity in their therapeutic targets and the ability to serve as adjuvants, increasing the effectiveness of pre-existing immune compounds. The design and development of new standardized protocols for…mehr

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Produktbeschreibung
Translational medicine addresses the gap between research and the clinical application of new discoveries. To efficiently deliver new drugs to care centers, a preclinical evaluation, both in vitro and in vivo, is required to ensure that the most active and least toxic compounds are selected as well as to predict clinical outcome.

Antimicrobial nanomedicines have been shown to have higher specificity in their therapeutic targets and the ability to serve as adjuvants, increasing the effectiveness of pre-existing immune compounds. The design and development of new standardized protocols for evaluating antimicrobial nanomedicines is needed for both the industry and clinical laboratory. These protocols must aim to evaluate laboratory activity and present models of pharmacokinetic-pharmacodynamic and toxicokinetic behavior that predict absorption and distribution. Likewise, these protocols must follow a theranostics approach, be able to detect promising formulations, diagnose the infectious disease, and determine the correct treatment to implement a personalized therapeutic behavior. Given the possibilities that nanotechnology offers, not updating to new screening platforms is inadequate as it prevents the correct application of discoveries, increasing the effect of the valley of death between innovations and their use.

This book is structured to discuss the fundamentals taken into account for the design of robust, reproducible and automatable evaluation platforms. These vital platforms should enable the discovery of new medicines with which to face antimicrobial resistance (RAM), one of the great problems of our time.
Autorenporträt
Dr. Bueno is currently 'Chief Scientific Officer' of  Research Center of Bioprospecting and Biotechnology for Biodiversity Foundation (BIOLABB). Researcher in Bioprospecting development and consulting. Doctor in medicine from Caldas University, Manizales, Colombia (2001). Master degree in biomedical sciences from Antioquia University, Medellín, Colombia (2008). Expert in design and implementation of antimicrobial platforms for to evaluate natural products and synthesis drugs with the aim of optimize in vitro antimicrobial activity selection of new chemical entities for future anti infective pharmaceutical, Bogotá, Colombia. Fellow, COLCIENCIAS-Universidad de Caldas (2002). Fellow of University of the United Nations in antifungal susceptibility testing, Instituto Nacional de Enfermedades Infecciosas, INEI.ANLIS, Buenos Aires, Argentina (2004). Fellow, International Visitor Leadership Program on "Public Health", United States Department of State, Bureau of Educational and Cultural Affairs (2012), 2221 KONUK VEYA AKADEM¿K ¿Z¿NL¿ (SABBAT¿CAL) B¿L¿M ¿NSANI DESTEKLEME PROGRAMI (2015). Award of Colombian Dermatology Association, Best research in dermatology (2006). Enrique Nuñez Olarte award for pharmacological research. Colombian Pharmacology Association (2009). Author of 50 articles in pharmacological research. Author in 13 chapter books in antimicrobial drug discovery and bioprospecting as well as the book titled 'MOLECULAR EVOLUTIONARY MODELS IN DRUG DISCOVERY'.