In vitro evaluation o f Transdermal Patch of Palonosetron for Antiemetic Therapy

Authors

  • Atul Tripathi University Institute of Pharmacy, Pt. Ravishankar Shukla University, Raipur
  • Piyush Tyagi College of Pharmacy, SSSUTMS, Sehore, M.P.
  • Amber Vyas University Institute of Pharmacy, Pt. Ravishankar Shukla University, Raipur
  • Beena Gidwani University Institute of Pharmacy, Pt. Ravishankar Shukla University, Raipur
  • Amol Chandekar School of Pharmacy & Research, Peoples University, Bhopal
  • Hemantkumar Sharma College of Pharmacy, SSSUTMS, Sehore, M.P.

Keywords:

Palonosetron, Transdermal Drug Delivery System, Serotonin 5-HT3 antagonist

Abstract

Skin is one of the routes for systemic delivery of drugs through various drug delivery system. A transdermal Drug Delivery System (TDDS) is one of the most reliable and useful system to deliver drug systemically through skin. Generally medicated patch is placed on skin for delivery of medication through it into the blood stream. The aim of present study was to formulate and evaluate Palonosetron transdermal patch in vitro that could be used for antiemetic therapy. The incorporation ofPalonosetron a serotonin 5-HT3 antagonist drug was envisaged. The TDDS was prepared by solvent evaporation technique and was evaluated for organoleptic characteristics and other physicochemical properties Thickness, Weight variation, Drug content uniformity, Tensile strength, % Elongation, Folding endurance & Moisture content. The in vitro permeation study of the patch was carried out through KesaryChein diffusion cell as barrier membrane. Phosphate buffer pH 7.4 was used as dissolution medium and the temperature was maintained at 37 ± 10C. The in vitro permeation study of the prepared patch indicated a time dependent increase in drug release throughout the study. The percentage of cumulative drug release was found to be 76.25% in 24 hours.The study shows a new approach to work in with Palonosetron.

References

. Prausnitz MR, Langer R. Transdermal

drug delivery. Nature biotechnology.

;26(11):1261-8.

. Chien YW, Swarbrick J. Novel drug

delivery systems. 1992.

. Naik A, Kalia YN, Guy RH.

Transdermal drug delivery:

overcoming the skin’s barrier function.

Pharmaceutical science & technology

today. 2000;3(9):318-26.

. Rajadhyaksha VJ. Penetration

enhancers for transdermal drug

delivery of systemic agents. Google

Patents; 1983.

. Singh J. Transdermal Drug Delivery

Formulation. Google Patents; 2006.

. Dhiman S, Singh TG, Rehni AK.

Transdermal patches: A recent

approch to new drug delivery system.

Int J Pharm Pharm Sci. 2011;3(5):26-

. Yadav V. Transdermal drug delivery

system: Review. International Journal

of Pharmaceutical Sciences and

Research. 2012;3(2):376.

. Klose KT-J, Zhou J, Morgan TM,

Finnin BC, Reed BL. Transdermal

delivery of antiemetics. Google

Patents; 2005.

. Boccia R, Grunberg S, FrancoGonzales E, Rubenstein E, Voisin D.

Efficacy of oral palonosetron

compared to intravenous

palonosetron for the prevention of

chemotherapy-induced nausea and

vomiting associated with moderately

emetogenic chemotherapy: a phase 3

trial. Supportive Care in Cancer.

;21(5):1453-60.

. Segal IS, Jarvis DJ, Duncan SR,

White PF, Maze M. Clinical efficacy of

oral-transdermal clonidine

combinations during the perioperative

period. Anesthesiology.

;74(2):220-5.

. Boekhorst J, Van Tol R. Catapres

transdermal therapeutic system (TTS)

for long-term treatment of

hypertension. Low dose oral and

transdermal therapy of hypertension:

Springer; 1985. p. 106-10.

. Anderson AR, Weikert ML, Crain JL.

Determining the most optimal stage

for embryo cryopreservation.

Reproductive biomedicine online.

;8(2):207-11.

. Prodduturi S, Sadrieh N, Wokovich

AM, Doub WH, Westenberger BJ,

Buhse L. Transdermal delivery of

fentanyl from matrix and reservoir

systems: effect of heat and

compromised skin. Journal of

pharmaceutical sciences.

;99(5):2357-66.

. Jamak V, Ghosh B, Desai B, Khanam

J. Recent trends in transdermal

cardiovascular therapy. Indian journal

of pharmaceutical sciences.

;68(5).

. Chaudhary H, Saini S, Singh G.

Formulation And Evaluation Of

Fexofenadine Hydrochloride

Transdermal Patch. Journal of Drug

Delivery and Therapeutics. 2012;2(5).

. Parashar T, Sachan R, Singh V,

Singh G, Tyagi S, Patel C, et al.

Ethosomes: A recent vesicle of

transdermal drug delivery system.

. Jain S, Mishra D, Kuksal A, Tiwary A,

Jain N. Vesicular approach for drug

delivery into or across the skin:

current status and future prospects.

Pharmacy Online. 2006;1:1-32.

. Kumar S, Nain P, Singh J. Nicotine

addiction and its Pharmacological

effects: A Review. 2011.

. Henningfield JE. Nicotine medications

for smoking cessation. New England

Journal of Medicine.

;333(18):1196-203.

. Lewis S, Udupa N. Design and

evaluation of matrix type and

membrane controlled transdermal

delivery systems of nicotine suitable

for use in smoking cessation. Indian

journal of pharmaceutical sciences.

;68(2).

. Jain SK, Vyas SP, Dixit V. Salbutamol

delivering transdermal dosage form

based on osmo-regulatory principle.

Drug Development and Industrial

Pharmacy. 1990;16(9):1565-77.

. Prabhakar D, Sreekanth J, Jayaveera

K. Transdermal drug delivery patches:

a review. Journal of Drug Delivery and

Therapeutics. 2013;3(4):231-21.

. Can AS, Erdal MS, Güngör S, Özsoy

Y. Optimization and characterization

of chitosan films for transdermal

delivery of ondansetron. Molecules.

;18(5):5455-71.

. Suryadevara P. Formulation and

Evaluation of antiemetic patch

comprising Ondansetron

hydrochloride. Rajiv Gandhi University

of Health Sciences, Karnataka,

Banglore. 2010;58.

. Reddy KR, Mutalik S, Reddy S. Oncedaily sustained-release matrix tablets

of nicorandil: formulation and in vitro

evaluation. AAPS pharmscitech.

;4(4):480-8.

. Haigh JM, Smith EW. The selection

and use of natural and synthetic

membranes for in vitro diffusion

experiments. European journal of

pharmaceutical sciences. 1994;2(5-

:311-30.

. Shah V, Raval S, Peer S, Upadhyay

U. A comparative evaluation of

different membranes for their diffusion

efficiency: an in vitro study. Pharma

Science Monitor-An International

Journal Pharmaceutical Sciences.

;1(1):41-9.

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Published

2017-12-31

How to Cite

Atul Tripathi, Piyush Tyagi, Amber Vyas, Beena Gidwani, Amol Chandekar, & Hemantkumar Sharma. (2017). In vitro evaluation o f Transdermal Patch of Palonosetron for Antiemetic Therapy. International Journal of Drug Delivery, 9(4), 119–124. Retrieved from https://ijdd.arjournals.org/index.php/ijdd/article/view/316

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