TY - JOUR
T1 - Topical non-aqueous nanoemulsion of Alpinia galanga extract for effective treatment in psoriasis
T2 - In vitro and in vivo evaluation
AU - Ramanunny, Arya Kadukkattil
AU - Wadhwa, Sheetu
AU - Kumar Singh, Sachin
AU - Kumar, Bimlesh
AU - Gulati, Monica
AU - Kumar, Ankit
AU - Almawash, Saud
AU - Al Saqr, Ahmed
AU - Gowthamarajan, Kuppusamy
AU - Dua, Kamal
AU - Singh, Harpreet
AU - Vishwas, Sukriti
AU - Khursheed, Rubiya
AU - Rahana Parveen, Shaik
AU - Venkatesan, Aravindhanathan
AU - Paudel, Keshav Raj
AU - Hansbro, Philip M.
AU - Kumar Chellappan, Dinesh
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/8/25
Y1 - 2022/8/25
N2 - Non-aqueous nanoemulsion (NANE) of Alpinia galanga extract (AGE) was prepared using Palmester 3595 (MCT oil) as oil phase, Cremophor RH 40-Transcutol P® as surfactant-co-surfactant (Smix), and glycerin as non-aqueous polar continuous phase. The composition was optimized by applying three-level, four factor Box-Behnken design (BBD). The mean droplet size and zeta potential of the optimized AGE NANE was found to be 60.81 ± 18.88 nm and −7.99 ± 4.14 mV, respectively. The ex vivo permeation studies of AGE NANE and AGE per se on porcine skin reported flux of 125.58 ± 8.36 µg/cm2 h−1 and 12.02 ± 1.64 µg/cm2 h−1, respectively. Therefore, the enhancement ratio has shown 10-folds increase in the flux for AGE NANE when compared to extract per se. Later, confocal laser scanning microcopy confirmed that AGE NANE were able to penetrate into skin's stratum by trans-follicular transport mechanism. The stability studies of AGE NANE confirmed its stability at 30 ± 2 °C/75 ± 5 % RH and 5 ± 3 °C. The efficacy of AGE NANE was evaluated in vivo on imiquimod (IMQ) induced mouse model. The mice treated with low and high doses of AGE NANE (groups VI and VII) showed significant (p < 0.05) amelioration of psoriasis. Results of histopathology indicated reduction in psoriasis area severity index in AGE NANE treated mice (group VI and group VII).
AB - Non-aqueous nanoemulsion (NANE) of Alpinia galanga extract (AGE) was prepared using Palmester 3595 (MCT oil) as oil phase, Cremophor RH 40-Transcutol P® as surfactant-co-surfactant (Smix), and glycerin as non-aqueous polar continuous phase. The composition was optimized by applying three-level, four factor Box-Behnken design (BBD). The mean droplet size and zeta potential of the optimized AGE NANE was found to be 60.81 ± 18.88 nm and −7.99 ± 4.14 mV, respectively. The ex vivo permeation studies of AGE NANE and AGE per se on porcine skin reported flux of 125.58 ± 8.36 µg/cm2 h−1 and 12.02 ± 1.64 µg/cm2 h−1, respectively. Therefore, the enhancement ratio has shown 10-folds increase in the flux for AGE NANE when compared to extract per se. Later, confocal laser scanning microcopy confirmed that AGE NANE were able to penetrate into skin's stratum by trans-follicular transport mechanism. The stability studies of AGE NANE confirmed its stability at 30 ± 2 °C/75 ± 5 % RH and 5 ± 3 °C. The efficacy of AGE NANE was evaluated in vivo on imiquimod (IMQ) induced mouse model. The mice treated with low and high doses of AGE NANE (groups VI and VII) showed significant (p < 0.05) amelioration of psoriasis. Results of histopathology indicated reduction in psoriasis area severity index in AGE NANE treated mice (group VI and group VII).
KW - Alpinia galanga extract
KW - Box-Behnken design
KW - Imiquimod induced mouse model
KW - Non-aqueous nanoemulsion
KW - PASI
UR - http://www.scopus.com/inward/record.url?scp=85132883428&partnerID=8YFLogxK
U2 - 10.1016/j.ijpharm.2022.121882
DO - 10.1016/j.ijpharm.2022.121882
M3 - Article
C2 - 35671853
AN - SCOPUS:85132883428
SN - 0378-5173
VL - 624
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
M1 - 121882
ER -