Alekha K. Dash

Prof. Dr. Alekha K. Dash


Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 1998 in Journal of Pharmacological and Toxicological Methods
Verified
Journal Article
Closed access
ADAlekha K. Dash
Alekha K. Dash
GCGreggreyC Cudworth
GreggreyC Cudworth

9 December 2009 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
Christopher J. DestacheChristopher J. Destache
Christopher J. Destache
TBTodd Belgum
Todd Belgum
KCKeith Christensen
Keith Christensen
ASAnnemarie Shibata
Annemarie Shibata
ASAkhilesh Sharma
Akhilesh Sharma
ADAlekha K. Dash
Alekha K. Dash
Combination antiretroviral (AR) therapy continues to be the mainstay for HIV treatment. However, antiretroviral drug nonadherence can lead to the development of resistance and treatment failure. We have designed nanoparticles (NP) that contain three AR drugs and characterized the size, shape, and surface charge. Additionally, we investigated the in vitro release of the AR drugs from the NP using peripheral blood mononuclear cells (PBMCs).

18 March 2008 in AAPS PharmSciTech
Verified
Journal Article
Closed access
PDF file
WTW. J. Trickler
W. J. Trickler
ANA. A. Nagvekar
A. A. Nagvekar
ADAlekha K. Dash
Alekha K. Dash


15 February 2021 in Therapeutic Delivery
Verified
Journal Article
Closed access
RSRachana Sapkota
Rachana Sapkota
ADAlekha K. Dash
Alekha K. Dash
The topical and transdermal routes of drug administration are long known to the field of pharmaceutics. These routes have been explored for the delivery of a wide range of therapeutic agents over c...

16 November 2018 in Therapeutic Delivery
Verified
Journal Article
Closed access
SDSuyash Deodhar
Suyash Deodhar
ADAlekha K. Dash
Alekha K. Dash
The poor pharmacokinetic parameters and low solubility of many anticancer therapeutics have warranted the use of drug-delivery systems such as liposomes. Overcoming some drawbacks of the conventional liposomes, targeted liposomal delivery by longer circulation time by addition of poly(ethylene glycol) to the liposomal surface and further adding specific ligands to achieve ligand selective retention and uptake has been introduced. PEGylated liposomes are the only second-generation liposomal formulations in clinical use and are now being challenged with the allergenic response they pose even in the treatment of naive patients. This article will review the challenges and hindrances in the use of long circulating liposomes and explore the opportunities to overcome this issue.