Indu Pal Kaur

Prof. Dr. Indu Pal Kaur

University Institute of Pharmaceutical Sciences (UIPS), Panjab University, Chandigarh 160014, India
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Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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1 January 2004 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
Indu Pal KaurIndu Pal Kaur
Indu Pal Kaur
AGAlka Garg
Alka Garg
ASAnil K. Singla
Anil K. Singla
DADeepika Aggarwal
Deepika Aggarwal

11 October 2010 in Molecular Nutrition & Food Research
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Journal Article
Closed access
PDF file
VKVandita Kakkar
Vandita Kakkar
SSSukhjit Singh
Sukhjit Singh
DSDinesh Singla
Dinesh Singla
Indu Pal KaurIndu Pal Kaur
Indu Pal Kaur

1 February 2002 in European Journal of Pharmaceutical Sciences
Verified
Journal Article
Closed access
Indu Pal KaurIndu Pal Kaur
Indu Pal Kaur
KCKanwaljit Chopra
Kanwaljit Chopra
ASAmarpreet Saini
Amarpreet Saini

15 October 2020 in Frontiers in Bioengineering and Biotechnology
Verified
Journal Article
Open access
PDF file
TGTanvi Gupta
Tanvi Gupta
JSJoga Singh
Joga Singh
SKSandeep Kaur
Sandeep Kaur
SSSimarjot Sandhu
Simarjot Sandhu
GSGurpal Singh
Gurpal Singh
Indu Pal KaurIndu Pal Kaur
Indu Pal Kaur
Curcumin, very rightly referred to as “a wonder drug” is proven to be efficacious in a variety of inflammatory disorders including cancers. Antiaging, anti-inflammatory, antioxidant, antitumor, chemosensitizing, P-gp efflux inhibiting, and antiproliferative activity are some of the striking features of curcumin, highlighting its importance in chemotherapy. Curcumin inhibits Bcl-2, Bcl-XL, VEGF, c-Myc, ICAM-1, EGFR, STAT3 phosphorylation, and cyclin D1 genes involved in the various stages of breast, prostate, and gastric cancer proliferation, angiogenesis, invasion, and metastasis. The full therapeutic potential of curcumin however remains under explored mainly due to poor absorption, rapid metabolism and systemic elimination culminating in its poor bioavailability. Furthermore, curcumin is insoluble, unstable at various pH and is also prone to undergo photodegradation. Nanotechnology can help improve the therapeutic potential of drug molecules with compromised biopharmaceutical profiles. Solid lipid nanoparticles (SLNs) are the latest offshoot of nanomedicine with proven advantages of high drug payload, longer shelf life, biocompatibility and biodegradability, and industrial amenability of the production process. We successfully developed CLEN (Curcumin encapsulated lipidic nanoconstructs) containing 15 mg curcumin per ml of the SLN dispersion with highest (till date, to our knowledge) increase in solubility of curcumin in an aqueous system by 1.4 × 106 times as compared to its intrinsic solubility of 11 ng/ml and high drug loading (15% w/v with respect to lipid matrix). Zero-order release kinetics observed for CLEN versus first order release for free curcumin establish controlled release nature of the developed CLEN. It showed 69.78 times higher oral bioavailability with respect to free curcumin; 9.00 times higher than a bioavailable marketed formulation (CurcuWIN®). The formulation showed 104, 13.3, and 10-times enhanced stability at pH 6.8, 1.2, and 7.4, respectively. All these factors ensure the efficacy of CLEN in treating cancer and other inflammatory diseases.

1 November 2014 in Journal of Controlled Release
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Journal Article
Closed access
Indu Pal KaurIndu Pal Kaur
Indu Pal Kaur
SKShilpa Kakkar
Shilpa Kakkar

1 November 2002 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
Indu Pal KaurIndu Pal Kaur
Indu Pal Kaur
RSR Smitha
R Smitha
DADeepika Aggarwal
Deepika Aggarwal
MKMona Kapil
Mona Kapil