Topical Formulation and in-Vitro Assessment of Moxifloxacin Hydrochloride Emulgel

Authors

  • Maysam M. Abass Faculty of Pharmacy, Department of Pharmaceutics, AL-Farahidi University, Baghdad, Iraq; Author

Keywords:

MOXF HCL, Emulgel, Cellulose derivative polymers

Abstract

Moxifloxacin HCL (MOXF HCL) was formulated as an emulgel dosage form in eight formulas using five main gel bases, carboxymethyl cellulose, hydroxypropyl methylcellulose, sodium alginate, sodium carboxy methyl cellulose, and a combination of hydroxypropyl methylcellulose and sodium alginate. The study revealed that the best emulgel base with accepted physical properties was CMC 2 %(w/w) in combined span 20 and tween 20 as surfactants compared with other cellulose derivative polymers, which gave us 97.85% of drug release. In contrast, HPMC gave us 76.5%, NaCMC gave us 57.83%, and Sod. Alginate gave us 64.92%, and HPMC/sod.alginate gave us 67.64%. Moreover, the Moxifloxacin HCL release from the selected formula in phosphate buffer pH 5.5 was increased as a result of growing surfactants used while increasing the liquid paraffin as an oil phase resulted in a decrease of drug release. On the other hand, the kinetic analysis of the amount of drug release from all Emulgel bases used showed mostly obeyed the Higuchi model. 

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References

Kshirsagar A., Drug Delivery Systems. Indian Journal of

Pharmacology, (2000), Vol.32, P. 54-61

Remington the Science and Practice of Pharmacy, 21st

edition, (2006), P.1658-1660

British pharmacopeia, vol. 1, London, (2001), P.302-315

Ansel H.C., Allen L.V., And Popovich N.G., Pharmaceutical

Dosage Forms and Drug Delivery Systems. 17th edition,

Lippincott Williams and walking's, chapter 10, (1999),

P.244-250.

Hameed RY, Nathir I, Abdulsahib WK, Almashhadani HA.

Study the effect of biosynthesized gold nanoparticles

on the enzymatic activity of alpha-Amylase. Research

Journal of Pharmacy and Technology. 2022 Aug1;15(8):3459-65.

Yehia I. Khalil, Lubna A.Sabri, Hala T. Sulayman, An

Investigation Release and Rheological Properties of

Miconazole Nitrate from Emulgel, Iraqi journal of

pharmaceutical science, 2009, Vol.18, 26-31.

Piemi M.Y., Korner D., Benita S., Marty J.P., Positively and

Negatively Charged Submicron Emulsion for Enhanced

Topical Delivery of Antifungal Drugs, Journal of

controlled Release, (1999), 58, 177-187.

Yvonne T.F., Khiany P., Al-Hanbali O., Effect of Carpobol

and Polyvinylpyrrolidone on Mechanical Rheological and

Release Properties of Bioadhesive Polyethylene Glycol

Gel, AASP, Pharm. Sci. Tech. (2000), article 24, P.1-3.

Masar B.M., Formulation and Evaluation of Meloxicam as a

Topical Preparation, Thesis, College of Pharmacy,

University of Baghdad, 2004.

Sellke M., Thomas R., Bayarri M.J., Berger J., Calibration of

p- values for testing precise null hypotheses, The

American Statistician, (2001)., chapter 5, P.62-71.

Capkova Z., Vitkova Z., Subova M., Formulation of

loratadine into Hydrogel, Acta Facult. Pharm. Univ.

Comenanae, (2007), 52, 73-78.

Ranga R. K., Padmalatha D., and Buri P., Influence of

molecular size and water solubility of the solute on its

release from swelling and erosion controlled polymeric

matrices, Journal of Controlled Release, (1990), Vol.12,

P.133-141.

Raju N.K., Velmurugan S. and Deepika B., Formulation and

In-Vitro Evaluation of Buccal Tablets of metoprolol

Tartrate, International Journal f Pharmacy and

Pharmaceutical Sciences,2011, Vol. 2, P.239-246.

Biswal D.R., Singh R.P., Characterisation of carboxymethyl

cellulose and polyacrylamide graft copolymer, Journal

of Controlled Release, (2004), article 57, P.379-387.

Moffat A.C., Clarke's Isolation and Identification of drugs,

rdeddition, London, pharmaceutics Society of Great

Britain, 2005, P.770-800.

Mohammed AK, Al-Shaheeb S, Fawzi OF, Almashhadani

HA, Kadhim MM. Evaluation of lnterlukein-6 and

Vitamin D in Patients with COVID-19. Research Journal

of Biotechnology Vol. 2022 Oct;17(10).

Silverstein R.M. and Webster F.X., Spectrometric

Identification of Organic Compounds, 6thedition, Jon

Wiley and Sons, (1998), P. 404-410.

Gao P., Skoug J. W., Nixon P. R., Ju T. R., Stemm N.L., and

Sung K. C., Sodium Alginate-Magnesium Aluminum

Silicate Composite Topical Gel; Behavior, viscosity and

Drug Diffusitvity, J. Pharm. Sci. 2007,85,P. 732-740.

Magdy I. M., Optimization of Chlorphenesin emulgel

formulation. American Association of Pharmaceutical

Scientists, (2004), article 6, P. 1-7.

Wan L., Viscosity Change in Salicylic Acid-Cetrimide

System by Surfactants, J.Pharm.Sci.,(1990), Vol.62,142-

Ban N.B., Cleland J.L., Yang J. and Manning M.C., Tween

Protects Recombinant Human Growth Hormone

against Agitation induced Damage via Hydrophobic

Interactions, J.Pharm.Sci.,(1998),87,P.1554-1559.

Katakam M., Bell L., Banga AK., The Effect of Surfactants

on the Physical Stability of Recombinant Human

Growth Hormone, journal of pharmaceutical sciences,

, article 84, vol. 6, P.713-788.

Higuchi W.I., Analysis of Data on the Medicament Release from Ointment, J.Pharm.Sci., (1962),51, P.802-804.

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Published

2023-04-30

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How to Cite

M. Abass, M. (2023). Topical Formulation and in-Vitro Assessment of Moxifloxacin Hydrochloride Emulgel. History of Medicine, 9(2). http://13.200.237.241/HOM/index.php/medicine/article/view/581