DEVELOPMENT AND CHARACTERIZATION OF PIPER RETROFRACTUM EXTRACT LOADED MUCOADHESIVE NANOSTRUCTURED LIPID CARRIERS FOR TOPICAL ORAL DRUG DELIVERY

Authors

  • Kavee Srichaivatana Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand
  • Anan Ounaroon Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand
  • Waree Tiyaboonchai bThe Center of Excellence for Innovation in Chemistry (PERCH-CIC), Commission on High Education, Ministry of Education, Thailand, cThe Center of Excellence in Medical Biotechnology, Naresuan University, Phitsanulok, Thailand

DOI:

https://doi.org/10.22159/ijpps.2017v9i9.19382

Keywords:

Nanostructured lipid carriers, Mucoadhesive, Piper retrofractum, Piperine

Abstract

Objective: To develop and characterize Piper retrofractum extract loaded nanostructured lipid carriers (PRE loaded NLCs) for topical oral cavity administration to enhance bioavailability and stability of piperine.

Methods: PRE loaded NLCs were prepared with a hot high-pressure homogenization technique followed by coating the particle surface with mucoadhesive polymers; polyethene glycol 400 (PEG) and polyvinyl alcohol (PVA). The physicochemical properties in terms of particle size, polydispersity index, zeta potential, drug entrapment efficiency, in vitro drug release profile and antimicrobial activities were examined. In vitro, mucoadhesion studies were assessed by the wash-off test. The physicochemical stabilities of mouth spray containing PRE loaded NLCs were investigated by kept at room temperature and 4 °C for 6 mo.

Results: The PRE loaded NLCs showed spherical shape with a mean particle size of ~100-120 nm and zeta potential of ~-24 mV. Up to 90% drug entrapment efficiency was achieved. PEG-NLCs and PVA-NLCs showed a strong interaction with porcine buccal mucosa than uncoated-NLCs. All PRE loaded NLCs formulations revealed fast release characteristics and effective against Streptococcus mutans and S. sanguinis. The mouth spray containing PRE loaded NLCs showed good physical stability without particle aggregation. In addition, the chemical stability of piperine in NLCs was significantly improved during storage at both storage conditions compared to its solution form.

Conclusion: The developed PRE loaded polymer coated-NLCs showed high potential to use as a local drug delivery system for reducing the bacterial growth in the oral cavity.

Downloads

Download data is not yet available.

References

Schmidt JC, Bux M, Filipuzzi-Jenny E, Kulik EM, Waltimo T, Weiger R, et al. Influence of time, toothpaste and saliva in the retention of Streptococcus mutans and Streptococcus sanguinis on different toothbrushes. J Appl Oral Sci 2014;22:152-8.

Spatafora G, Rohrer K, Barnard D, Michalek S. A Streptococcus mutans mutant that synthesize elevated levels of the intracellular polysaccharide is hypercariogenic in vivo. Infect Immun 1995;63:2556-63.

Kolenbrander PE, Palmer RJ, Periasamy S, Jakubovics NS. Oral multi species biofilm development and the key role of cell-cell distance. Nat Rev Microbiol 2010;8:471-80.

Zanela NL, Bijella MF, Rosa OP. The influence of mouthrinses with antimicrobial solutions on the inhibition of dental plaque and on the levels of mutans streptococci in children. Pesqui Odontol Bras 2002;16:101-6.

Eley BM. Antibacterial agents in the control of supragingival plaque-a review. Br Dent J 1999;186:286-96.

Tombes MB, Gallucci B. The effects of hydrogen peroxide rinses on the normal oral mucosa. Nurs Res 1993;42:332-7.

Dwivedi D, Singh V. Effects of the natural compounds embelin and piperine on the biofilm-producing property of Streptococcus mutans. Afr J Tradit Complementary Altern Med 2016;6:57-61.

Aneja KR, Joshi R, Sharma C, Aneja A. Antimicrobial efficacy of fruit extracts of two piper species against selected bacterial and oral fungal pathogens. Braz J Oral Sci 2010;9:421-6.

Fang L, Wang L, Yao Y, Zhang J, Wu X, Li X, et al. Micro-and nano-carrier systems: the noninvasive and painless local administration strategies for disease therapy in mucosal tissues. Nanomedicine 2017;13:153-71.

Aher SS, Malsane ST, Saudagar RB. Nanosuspension: an overview. Int J Curr Pharm Res 2017;9:19-23.

Huang Y, Leobandung W, Foss A, Peppas NA. Molecular aspects of muco-and bioadhesiom: tethered structures and site-specific surfaces. J Controlled Release 2000;65:63-71.

Popov A, Enlow E, Bourassa J, Chen H. Mucus-penetrating nanoparticles made with "mucoadhesive" polyvinyl alcohol. Nanomedicine 2016;12:1863-71.

Rabanel JM, Hildgen P, Banquy X. Assessment of PEG on polymeric particles surface, a key step in drug carrier translation. J Controlled Release 2014;185:71-87.

Bajad S, Singla AK, Bedi KL. Liquid chromatographic method for determination of piperine in rat plasma: application to pharmacokinetics. J Chromatogr B 2002;776:245-9.

Gref R, Domb A, Quellec P, Blunk T, Müller RH, Verbavatz JM, et al. The controlled intravenous delivery of drugs using PEG-coated sterically stabilized nanospheres. Adv Drug Delivery Rev 1995;16:215-33.

Acar HY, Garaas RS, Syud F, Bonitatebus P, Kulkarni AM. Superparamagnetic nano particles stabilized by polymerized PEGylated coatings. J Magn Magn Mater 2005;293:1-7.

Matsui H, Wagner VE, Hill DB, Schwab UE, Rogers TD, Button B, et al. A physical linkage between cystic fibrosis airway surface dehydration and Pseudomonas aeruginosa biofilms. Proc Natl Acad Sci USA 2006;103:18131-6.

Dawson M, Wirtz D, Hanes J. Enhanced viscoelasticity of human cystic fibrotic sputum correlates with increasing micro heterogeneity in particle transport. J Biol Chem 2003;278:50393-401.

Yang M, Lai SK, Yu T, Wang YY, Happe C, Zhong W, et al. Nanoparticle penetration of human cervicovaginal mucus: the effect of polyvinyl alcohol. J Controlled Release 2014;192:202-8.

Müller RH, Radtke M, Wissing SA. Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) in cosmetic and dermatological preparations. Adv Drug Delivery Rev 2002;54 Suppl 1:131-55.

Makadia HK, Siegel SJ. Poly lactic-co-glycolic acid (PLGA) as biodegradable controlled drug delivery carrier. Polymers (Basel) 2011;3:1377-97.

Fontana G, Licciardi M, Mansueto S, Schillaci D, Giammona G. Amoxicillin-loaded poly ethyl cyanoacrylate nanoparticles: influence of PEG coating on the particle size, drug release rate and phagocytic uptake. Biomaterials 2001;22:2857-65.

Ahn SJ, Lee SJ, Kook JK, Lim BS. Experimental anti microbial orthodontic adhesives using nanofillers and silver nanoparticles. Dent Mater 2009;25:206-13.

Chávez de Paz LE, Resin A, Howard KA, Sutherland DS, Wejse PL. Antimicrobial effect of chitosan nanoparticles on Streptococcus mutans biofilms. Appl Environ Microbiol 2011;77:3892-5.

Jenning V, Thünemann AF, Gohla SH. Characterisation of a novel solid lipid nanoparticle carrier system based on binary mixtures of liquid and solid lipids. Int J Pharm 2000;199:167-77.

Jenning V, Schäfer-Korting M, Gohla SH. Vitamin loaded solid lipid nanoparticles for topical use: drug release properties. J Controlled Release. 2000;66:115-26.

Helgason T, Awad TS, Kristbergsson K, McClements DJ, Weiss J. Influence of polymorphic transformations on gelation of tripalmitin solid lipid nanoparticle suspensions. J Am Oil Chem Soc 2008;85:501-11.

Kotte SCB, Dubey PK, Murali PM. Identification and characterization of stress degradation products of piperine and profiling of a black pepper (Piper nigrum L.) extract using LC/Q-TOF-dual ESI-MS. Anal Methods 2014;6:8022-9.

Published

01-09-2017

How to Cite

Srichaivatana, K., A. Ounaroon, and W. Tiyaboonchai. “DEVELOPMENT AND CHARACTERIZATION OF PIPER RETROFRACTUM EXTRACT LOADED MUCOADHESIVE NANOSTRUCTURED LIPID CARRIERS FOR TOPICAL ORAL DRUG DELIVERY”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 9, no. 9, Sept. 2017, pp. 79-86, doi:10.22159/ijpps.2017v9i9.19382.

Issue

Section

Original Article(s)