TY - JOUR
T1 - Breaking the barriers for the delivery of amikacin
T2 - Challenges, strategies, and opportunities
AU - Maxwell, Amala
AU - Ghate, Vivek
AU - Aranjani, Jesil
AU - Lewis, Shaila
N1 - Funding Information:
The authors are grateful to the All-India Council for Technical Education (AICTE), New Delhi, India, for providing financial assistance in the form of National Doctoral Fellowship (NDF) to Amala Maxwell [File No. 1-6190129051]. The authors also thank Manipal College of Pharmaceutical Sciences and Manipal Academy of Higher Education (MAHE), Manipal, India, for providing Intramural funds and facilities for the research.
Funding Information:
The authors are grateful to the All-India Council for Technical Education ( AICTE ), New Delhi, India, for providing financial assistance in the form of National Doctoral Fellowship (NDF) to Amala Maxwell [File No. 1-6190129051 ]. The authors also thank Manipal College of Pharmaceutical Sciences and Manipal Academy of Higher Education (MAHE), Manipal, India, for providing Intramural funds and facilities for the research.
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2021/11/1
Y1 - 2021/11/1
N2 - Hypodermic delivery of amikacin is a widely adopted treatment modality for severe infections, including bacterial septicemia, meningitis, intra-abdominal infections, burns, postoperative complications, and urinary tract infections in both paediatric and adult populations. In most instances, the course of treatment requires repeated bolus doses of amikacin, prolonged hospitalization, and the presence of a skilled healthcare worker for administration and continuous therapeutic monitoring to manage the severe adverse effects. Amikacin is hydrophilic and exhibits a short half-life, which further challenges the delivery of sufficient systemic concentrations when administered by the oral or transdermal route. In this purview, the exploitation of novel controlled and sustained release drug delivery platforms is warranted. Furthermore, it has been shown that novel delivery systems are capable of increasing the antibacterial activity of amikacin at lower doses when compared to the conventional formulations and also aid in overcoming the development of drug-resistance, which currently is a significant threat to the healthcare system worldwide. The current review presents a comprehensive overview of the developmental history of amikacin, the mechanism of action in virulent strains as well as the occurrence of resistance, and various emerging drug delivery solutions developed both by the academia and the industry. The examples outlined within the review provides significant pieces of evidence on novel amikacin formulations in the field of antimicrobial research paving the path for future therapeutic interventions that will result in improved clinical outcome.
AB - Hypodermic delivery of amikacin is a widely adopted treatment modality for severe infections, including bacterial septicemia, meningitis, intra-abdominal infections, burns, postoperative complications, and urinary tract infections in both paediatric and adult populations. In most instances, the course of treatment requires repeated bolus doses of amikacin, prolonged hospitalization, and the presence of a skilled healthcare worker for administration and continuous therapeutic monitoring to manage the severe adverse effects. Amikacin is hydrophilic and exhibits a short half-life, which further challenges the delivery of sufficient systemic concentrations when administered by the oral or transdermal route. In this purview, the exploitation of novel controlled and sustained release drug delivery platforms is warranted. Furthermore, it has been shown that novel delivery systems are capable of increasing the antibacterial activity of amikacin at lower doses when compared to the conventional formulations and also aid in overcoming the development of drug-resistance, which currently is a significant threat to the healthcare system worldwide. The current review presents a comprehensive overview of the developmental history of amikacin, the mechanism of action in virulent strains as well as the occurrence of resistance, and various emerging drug delivery solutions developed both by the academia and the industry. The examples outlined within the review provides significant pieces of evidence on novel amikacin formulations in the field of antimicrobial research paving the path for future therapeutic interventions that will result in improved clinical outcome.
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U2 - 10.1016/j.lfs.2021.119883
DO - 10.1016/j.lfs.2021.119883
M3 - Review article
AN - SCOPUS:85112846132
SN - 0024-3205
VL - 284
JO - Life Sciences
JF - Life Sciences
M1 - 119883
ER -