Amphotericin B microspheres: a therapeutic approach to minimize toxicity while maintaining antifungal efficacy.J Microencapsul. 2009 Nov; 26(7):580-7.JM
Abstract
Amphotericin B microsphere formulations with and without addition of polyethylene glycol 2000 in cross-linked bovine serum albumin were prepared. Amphotericin B microspheres were characterized for particle size (<5 microm), zeta potential (approximately 30 mV) and drug interaction by DSC and FTIR and were found to be stable formulations. Drug release profiles for these microspheres revealed that the release was primarily by diffusion. In vitro toxicity as assessed by release of haemoglobin and potassium demonstrated no toxic effect as compared with conventional solution formulation. Antifungal activity in vitro was comparable to solution formulation when tested by broth dilution method.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
19839793
Citation
Angra, Pawan K., et al. "Amphotericin B Microspheres: a Therapeutic Approach to Minimize Toxicity While Maintaining Antifungal Efficacy." Journal of Microencapsulation, vol. 26, no. 7, 2009, pp. 580-7.
Angra PK, Oettinger C, Balakrishna Pai S, et al. Amphotericin B microspheres: a therapeutic approach to minimize toxicity while maintaining antifungal efficacy. J Microencapsul. 2009;26(7):580-7.
Angra, P. K., Oettinger, C., Balakrishna Pai, S., & D'Souza, M. J. (2009). Amphotericin B microspheres: a therapeutic approach to minimize toxicity while maintaining antifungal efficacy. Journal of Microencapsulation, 26(7), 580-7. https://doi.org/10.3109/02652040902797516
Angra PK, et al. Amphotericin B Microspheres: a Therapeutic Approach to Minimize Toxicity While Maintaining Antifungal Efficacy. J Microencapsul. 2009;26(7):580-7. PubMed PMID: 19839793.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Amphotericin B microspheres: a therapeutic approach to minimize toxicity while maintaining antifungal efficacy.
AU - Angra,Pawan K,
AU - Oettinger,Carl,
AU - Balakrishna Pai,S,
AU - D'Souza,Martin J,
PY - 2009/10/21/entrez
PY - 2009/10/21/pubmed
PY - 2010/2/18/medline
SP - 580
EP - 7
JF - Journal of microencapsulation
JO - J Microencapsul
VL - 26
IS - 7
N2 - Amphotericin B microsphere formulations with and without addition of polyethylene glycol 2000 in cross-linked bovine serum albumin were prepared. Amphotericin B microspheres were characterized for particle size (<5 microm), zeta potential (approximately 30 mV) and drug interaction by DSC and FTIR and were found to be stable formulations. Drug release profiles for these microspheres revealed that the release was primarily by diffusion. In vitro toxicity as assessed by release of haemoglobin and potassium demonstrated no toxic effect as compared with conventional solution formulation. Antifungal activity in vitro was comparable to solution formulation when tested by broth dilution method.
SN - 1464-5246
UR - https://www.unboundmedicine.com/medline/citation/19839793/Amphotericin_B_microspheres:_a_therapeutic_approach_to_minimize_toxicity_while_maintaining_antifungal_efficacy_
L2 - https://www.tandfonline.com/doi/full/10.3109/02652040902797516
DB - PRIME
DP - Unbound Medicine
ER -