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July 05-06, 2019 | Paris, France

Pharmaceutics and Advanced Drug Delivery Systems

2

nd

International Conference and Exhibition on

Asian Journal of Biomedical and Pharmaceutical Sciences | ISSN:2249-622X | Volume 9

Dual loaded actively targeted liposomes for anti-resistance treatment of melanoma

Harshita Mishra

1

, Sushama Talegaonkar

1,2

, Zeenat Iqbal

1

and

Manu Jaggi

3

1

Jamia Hamdard University, India

2

Delhi Pharmaceutical Sciences and Research University, India

3

Dabur Research Foundation, India

M

elanoma is one of the deadliest cancers with very

low response and survival rates. Main reason of poor

outcomes of therapy is the inherent resistance of melanoma

cells.Survivinisaproteinwhichisoverexpressedbymelanoma

cells and is known to impart resistance to them against

apoptosis which is supposed to be induced by chemotherapy.

Eugenol has been reported to inhibit survivin in breast cancer

cells. Thus, in order to fight resistant melanoma in a more

efficient manner, we formulated hyaluronic acid (HA) coated

liposomes loaded with eugenol along with dacrabazine

which is the gold standard chemotherapeutic agent used for

melanoma treatment. After synthesizing the liposomes using

solvent injection method, QbD was applied to optimize and

obtain a final formulation with desired quality attributes. The

optimized formulation was then subjected to performance

analysis in cell lines and animals. Coated-Dacarbazine Eugenol

Liposomes were found to possess almost 9 folds more

cytotoxicity than dacarbazine solution against melanoma cell

lines (at dacarbazine concentration of 0.5 µg/ml). The number

of late apoptotic cells was also found to be much higher

in formulation treated cells in comparison to dacarbazine

solution treated cells. Migration assay and proliferation study

also indicated towards considerably greater inhibition of cell

migration and proliferation by Coated-Dacarbazine Eugenol

Liposomes, signifying its potential against metastasis. Results

of pharmacodynamic study on melanoma bearing C57BL/6

mice revealed that our formulation could significantly delay

the tumor growth in comparison to dacarbazine solution; and

biodistribution study confirmed the long circulating nature of

theformulation.Thus,theresultsofthisstudyindicatetowards

better possibilities of melanoma treatment if the treatment is

focusedonspecificresistancemechanismofthisdeadlycancer.

Speaker Biography

Harshita Mishra is about to finish her doctorate in Pharmaceutics from

Jamia Hamdard University, India. She has 14 international publications

and around 300 citations. She has also written 5 book chapters in

books edited by Elsevier, Stanford etc. Her educational background

includes Bachelor of Pharmacy, Master of Pharmacy and Post Graduate

Diploma in Intellectual Property Rights. She is a two times qualifier of

GPAT which is an all India level aptitude and evaluation exam. She has

twice received Elsevier’s ‘Top 25 Hottest Articles’ award for her paper

on metal nanoparticles. She has presented papers in 7 International

and National Conferences and won awards in 3 of them. Her areas of

interest include Nanotechnology and Cancer treatment.

e:

harshitasharma1088@gmail.com

Notes:

Harshita Mishra et al.

, Asian J Biomed Pharmaceut Sci, | ISSN: 2249-622X

Volume 9