FORMULATION AND CHARACTERIZATION OF ASCORBYL PALMITATE LOADED O/W MICROEMULSION

Authors

  • Rachmat Mauludin School of Pharmacy, Bandung Institute of Technology, Ganesha 10 Bandung, Indonesian
  • Siti Farhanah B. T. Mohamad School of Pharmacy, Bandung Institute of Technology, Ganesha 10 Bandung, Indonesian
  • Tri Suciati School of Pharmacy, Bandung Institute of Technology, Ganesha 10 Bandung, Indonesian

Keywords:

Ascorbyl palmitate, Microemulsion, Antioxidant, Physical, Chemical stability

Abstract

Objective: Ascorbyl palmitate (AP) is an effective free radical-scavenging antioxidant which promotes skin health and vitality. Besides that, AP helps to enhance the synthesis of collagen. Moreover, AP helps to reduced UVB that can induce erythema (sunburn). However, AP relatively unstable and tend to undergo oxidation and sensitive to light. According to literature study, solid lipid nanoparticle (SLN) and nanostructured lipid carrier (NLC) was used to protect AP against chemical degradation, but it was found that AP still had degraded and those preparations could not protect against chemical degradation. As an alternative, oil-in water microemulsion was formulated in order to find suitable formulation that can protect AP from chemical degradation.

Methods: The physicochemical properties of microemulsion were characterized and the antioxidant activity of AP was also determined. Component of microemulsion formula consists of AP, tween 80 as surfactant, propylene glycol and ethanol as cosurfactant, capric/caprylic triglyceride as oil phase and water. Optimization of AP, oil phase concentration and ratio of mixture of surfactant and co-surfactant were conducted. The physical stability evaluation includes organoleptic, pH and viscosity, globule size, freeze-thaw test and centrifugation determination. For chemical stability studies, remaining concentration of AP was determined using High Performance Liquid Chromatography (HPLC). Besides that, antioxidant activity of AP was determined by measuring the decreased intensity of purple colour DPPH using UV spectrophotometry.

Results: There is no significant change in terms of organoleptic of AP o/w microemulsion for all formulation. In terms of physical stability, AP o/w microemulsion was found to remain stable up to 30 days in the real time. Based on pH determination results, AP tend to become acidic after when stored at room temperature after 60 days. Resulted microemulsions showed a good physical stability after freeze-thaw test and centrifugation test. The globule size of microemulsion especially formulation C9 remained stable up to 60 days when stored at room temperature and after 6th cycle of freeze-thaw test. Although AP was formulated in microemulsion, but the effectiveness of 1% of AP loaded o/w microemulsion as an antioxidant was comparable to 1% solution of AP in methanol. The antioxidant activity of AP increased with increasing concentration. According to chemical stability test data, AP microemulsion undergoes major degradation when stored at temperature 25oC and 40oC. Meanwhile, it was seen that AP more stable when stored at temperature 40.

Conclusion: Hence, oil in water microemulsion could be generated with good physical stability and remain stable for 30 days in real time. However, microemulsion as a carrier was insufficient to chemically protect AP against chemical degradation. C. The product of AP when undergoes oxidation degradation are dehydroascorbic acid and 2, 3-diketo-gluconic acid. 

Downloads

Download data is not yet available.

References

Rowe RC, PJ Sheskey, PJ Weller. Handbook of Pharmaceutical Excipient, Fourth edition. The Pharmaceutical Press: London; 2003. p. 18-9, 51-3, 580-2, 802-3.

Ǖner M, Wissing SA, Yener G, Müller RH. Solid lipid nanoparticles(SLN) and nanostrutured lipid carriers (NLC) for application of ascorbyl palmitate. Pharmazie 2005;60:577–82.

Veerawat Teeranachaideekul, Rainer H Müller. Encapsulation of ascorbyl palmitate in nanostructured lipid carriers (NLC)—Effects of formulation parameters on physicochemical stability. Int J Pharm 2007;340:198–206.

Rachmat Mauludin, Rainer H Müller. Physicochemical Properties of Hesperidin Nanocrystal. Int J Pharm Pharm Sci 2013;5(Suppl 3):954-60.

Date AA, Naik B, Nagarsenker MS. Novel Drug Delivery Systems: Potential in Improving Topical Delivery of Antiacne Agents. Skin Pharmacology and Physiology 2006;19:2-16.

ED Goddard, B Vincent (eds). Polymer Adsorption and Dispersion Stability. ACS Symposium Series 240, America Chemical Society, Washington DC 1984.

Lachman L, HA MM Rieger, Gilbert S Banker. Pharmaceutical Dosage Forms, Disperse system. Marcel Dekker Inc 1998;1:245-52.

Blois MS. Antioxidant determinations by the use of a stable free radical. Nature 1958;29:1199-200.

Ankita Yadav, Richa Bhardwaj Sharma. Free radical scavenging potential of the solanum surattense burm f. An important medicinal plant. Int J Pharm Pharm Sci 2014;6(3):39-42.

Francesca Giuffrida, Frédéric Destaillats. Activity and thermal stability of antioxidants by differential scanning calorimetry and electron spin resonance spectroscopy, Department of Food Science, Royal Veterinary and Agricultural University, Frederiksberg C, Denmark 2006;101(3):1108-14.

Martin A. Physical Pharmacy, Fourth Edition; B. I. Waverly Pvt. Ltd. New York: 1994. p. 495 – 6.

Spiclin P, Gasperlin M, Kmetec V. Stability of ascorbyl palmitate in topical microemulsions Int J Pharm 2001;222:271–9.

Alexander T, Florence, David Attwood. Emulsion, suspensions and other disperse systems, in: Physicochemical Principles of Pharmacy, Pharmaceutical Press Fifth edition; 2011. p. 255.

Published

01-09-2014

How to Cite

Mauludin, R., S. F. B. T. Mohamad, and T. Suciati. “FORMULATION AND CHARACTERIZATION OF ASCORBYL PALMITATE LOADED O/W MICROEMULSION”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 6, no. 9, Sept. 2014, pp. 294-8, https://journals.innovareacademics.in/index.php/ijpps/article/view/2120.

Issue

Section

Original Article(s)