Development, optimization, and characterization of a novel tea tree oil nanogel using response surface methodology. (1st September 2016)

• Record Type: Journal Article
• Authors: Sinha, Priyam; Srivastava, Shruti; Mishra, Nidhi; Singh, Dhananjay Kumar; Luqman, Suaib; Chanda, Debabrata; Yadav, Narayan Prasad
• Is Part Of: Drug development and industrial pharmacy. Volume 42:Number 9(2016:Sep.)
• Page Start: 1434
• Page End: 1445
• Publication Date: 2016-09-01
• Subjects: Emulgel -- nanoemulsion -- particle size -- permeability -- tea tree oil -- texture analysis; Pharmaceutical chemistry -- Periodicals; Pharmaceutical industry -- Periodicals; Drug Industry -- Periodicals; Technology, Pharmaceutical -- Periodicals; 615.05
• DOI: 10.3109/03639045.2016.1141931
• Languages: English
• ISSNs: 0363-9045

Abstract

Abstract: Purpose: To develop and optimize nanoemulsion (NE)-based emulgel (EG) formulation as a potential vehicle for topical delivery of tea tree oil (TTO). Methodology: Central composite design was adopted for optimizing the processing conditions for NE preparation by high energy emulsification method viz. surfactant concentration, co-surfactant concentration, and stirring speed. The optimized NE was developed into emulgel (EG) using pH sensitive polymer Carbopol 940 and triethanolamine as alkalizer. The prepared EG was evaluated for its pH, viscosity, and texture parameters, ex vivo permeation at 37 °C and stability. Antimicrobial evaluation of EG in comparison to conventional gel and pure TTO was also carried out against selected microbial strains. Results and discussion: Optimized NE had particle size and zeta potential of 16.23 ± 0.411 nm and 36.11 ± 1.234 mV, respectively. TEM analysis revealed the spherical shape of droplets. The pH of EG (5.57 ± 0.05 ) was found to be in accordance with the range of human skin pH. EG also illustrated efficient permeation (79.58 μL/cm 2 ) and flux value (JSS ) of 7.96 μL cm 2 /h through skin in 10 h. Viscosity and texture parameters, firmness (9.3 ± 0.08 g), spreadability (2.26 ± 0.06 mJ), extrudability (61.6 ± 0.05 mJ), and adhesiveness (8.66 ± 0.08 g) depict its suitability for topical application. Antimicrobial evaluation of EG with same amount of TTO as conventional gel revealed broader zones of growth inhibitions against all the selected microbial strains. Moreover, EG was also found to be nonirritant (PII 0.0833). These parameters were consistent over 90 d. Conclusion: TTO EG turned out to be a promising vehicle for the topical delivery of TTO with enhanced therapeutic efficacy.