Development and Characterization of Barbaloin Gel for the Safe and Effective Treatment of Psoriasis

Authors

  • Navdeep Singh Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India
  • Kamya Goyal Department of pharmaceutical Analysis and Chemistry, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India
  • Shivi Sondhi Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India
  • Shammy Jindal Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Abstract

Psoriasis is an inflammatory skin disease which cause inflammation to the skin and generally the symptoms includes white or red colour of irregular skin; the patches are developed and they are commonly itchy and scaly to the skin. Barbaloin is an herbal phytoconstituent which is obtained from the plant aloe vera leaf part. In the present study hydrogels formulation batches from F1 to F10 were prepared by using carbopol 934, Xanthan gum, carbopol 940, and carbopol 71G NF as a gelling agent. The prepared formulations from F1 to F10 were evaluated for their physical appearance, Grittiness, spreadability, Homogeneity, viscosity, pH, swelling index and microscopical evaluation. The changes in each evaluation parameter were examined at multiples concentration of each polymer. The effects of gelling agent in each formulation were observed and it will help us to justify the suitable range of polymer as a single or in combination with other gelling agent. From these studies it was found to be formulation F2, F4, F7 and F10 showing good gelling properties and further these four formulations are selected for In Vitro drug release studies. By In Vitro drug release kinetics study formulation F2 and F10 showed higher release as compared to F4 and F7. Furthermore, formulation F2 and F7 had good kinetic release study and showed non fickian drug release as the n value was between 0.8-0.9. Therefore, from the above release study parameters formulation F2 and F10 show the best optimized release characterstics as compare to the selected optimized formulations F4 and F7.

Keywords: Psoriasis, Barbaloin, Hydrogel, Formulation and Evaluation.

Keywords:

Psoriasis, Barbaloin, Hydrogel, Formulation and Evaluation

DOI

https://doi.org/10.22270/jddt.v10i5.4299

Author Biographies

Navdeep Singh, Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Kamya Goyal, Department of pharmaceutical Analysis and Chemistry, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Department of pharmaceutical Analysis and Chemistry, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Shivi Sondhi, Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Shammy Jindal, Department of Pharmaceutics, Laureate Institute of Pharmacy, Kathog, Jawalamukhi, Himachal Pradesh 176031, India

Research scholar, Department of Pharmaceutics, Amity Institute of Pharmacy, Amity University Uttar Pradesh, Sector-125, Noida 201303, India

References

Menter A, Korman NJ, Elmets CA, Feldman SR, Gelfand JM, Gordon KB, Gottlieb A, Koo JY, Lebwohl M, Leonardi CL, Lim HW, “Guidelines of care for the management of psoriasis and psoriatic arthritis: section 6” Journal of the American Academy of Dermatology, 2011; 65(1):137-74.

Shrivastav S, Sindhu R, Kumar S, Kumar P, “Anti-psoriatic and phytochemical evaluation of Thespesia populnea bark extracts” Int J Pharm Sci, 2009; 1(1).

Rapp SR, Feldman SR, Exum ML, Fleischer Jr AB, Reboussin DM, “Psoriasis causes as much disability as other major medical diseases” Journal of the American Academy of Dermatology, 1999; 41(3):401-7.

Griffiths CE, Vander Walt JM, Ashcroft DM, Flohr C, Naldi L, Nijsten T, Augustin M, “The global state of psoriasis disease epidemiology: a workshop report” British Journal of Dermatology, 2017; 177(1):4-7.

Singh KK, Tripathy S, “Natural treatment alternative for psoriasis: a review on herbal resources” Journal of Applied Pharmaceutical Science, 2014; 4(11):114-21.

Patel DK, Patel K, Tahilyani V, “Barbaloin: a concise report of its pharmacological and analytical aspects” Asian Pacific journal of tropical biomedicine, 2012; 2(10):835-8.

Sánchez M, González-Burgos E, Iglesias I, Gómez-Serranillos MP, “Pharmacological update properties of Aloe vera and its major active constituents” Molecules, 2020; 25(6):1324

Tabata Y, “Biomaterial technology for tissue engineering applications” Journal of the Royal Society interface, 2009; 6(3):311-24.

McGhie AR, Chiu J, Fair PG, Blaine RL, “Thermogravimetric apparatus temperature calibration using melting point standards” Thermochimica acta, 1983; 67(2-3):241-50.

Bannan CC, Calabró G, Kyu DY, Mobley DL, “Calculating partition coefficients of small molecules in octanol/water and cyclohexane/water” Journal of chemical theory and computation, 2016; 12(8):4015-24.

Bele AA, Khale A, “An overview on thin layer chromatography” International Journal of Pharmaceutical Sciences and Research, 2011; 2(2):256.

Dent G, “Preparation of Samples for IR spectroscopy as KBr disks” Internet Journal of Vibrational Spectroscopy, 1996; 1:1-2.

Rote AR, Kumbhoje PA, Bhambar RS, “UV-visible spectrophotometric simultaneous estimation of paracetamol and nabumetone by AUC method in combined tablet dosage form” Pharmaceutical methods, 2012; 3(1):40-3.

Ahmed S, Mustaan N, Sheraz MA, un Nabi SA, Ahmad I, “Validation of a UV spectrometric method for the assay of tolfenamic acid in organic solvents” Journal of pharmaceutics, 2015.

Behera S, Ghanty S, Ahmad F, Santra S, Banerjee S, “UV-visible spectrophotometric method development and validation of assay of paracetamol tablet formulation” J Anal Bioanal Techniques, 2012; 3(6):151-7.

Queiroz MB, Marcelino NB, Ribeiro MV, Espindola LS, Cunha FR, Silva MV, “Development of gel with Matricaria recutita L. extract for topic application and evaluation of physical-chemical stability and toxicity” Lat. Am. J. Pharm, 2009; 28(4):574-9.

Nayak SH, Nakhat PD, Yeole PG, “Development and evaluation of cosmeceutical hair styling gels of ketoconazole” Indian journal of pharmaceutical sciences, 2005; 67(2):231.

Nandgude T, Thube R, Jaiswal N, Deshmukh P, Chatap V, Hire N, “Formulation and evaluation of pH induced in-situ nasal gel of salbutamol sulphate” International journal of pharmaceutical sciences and nanotechnology, 2008; 1(2):177-83.

Lee Y, Kim DN, Choi D, Lee W, Park J, Koh WG, “Preparation of interpenetrating polymer network composed of poly (ethylene glycol) and poly (acrylamide) hydrogels as a support of enzyme immobilization” Polymers for Advanced Technologies, 2008; 19(7):852-8.

Jain BD, “Formulation development and evaluation of Fluconazole gel in various polymer bases” Asian Journal of Pharmaceutics, 2016; 1(1).

Kumar L, Verma R, “In vitro evaluation of topical gel prepared using natural polymer” International journal of drug delivery, 2010; 2(1).

Published

15-09-2020
Statistics
Abstract Display: 1011
PDF Downloads: 861

How to Cite

1.
Singh N, Goyal K, Sondhi S, Jindal S. Development and Characterization of Barbaloin Gel for the Safe and Effective Treatment of Psoriasis. J. Drug Delivery Ther. [Internet]. 2020 Sep. 15 [cited 2025 May 25];10(5):188-97. Available from: https://www.jddtonline.info/index.php/jddt/article/view/4299

How to Cite

1.
Singh N, Goyal K, Sondhi S, Jindal S. Development and Characterization of Barbaloin Gel for the Safe and Effective Treatment of Psoriasis. J. Drug Delivery Ther. [Internet]. 2020 Sep. 15 [cited 2025 May 25];10(5):188-97. Available from: https://www.jddtonline.info/index.php/jddt/article/view/4299