Formulation and Characterization Liposome of Oxcarbazepine

Dina Permata Wijaya, Budi Untari, Herlina Herlina, Putri Siti Rahayu

Abstrak


Oxcarbazepine (OXC) was used as first line therapy or additional therapy for treatment of partial
and secondary of seizures. The penetration of OXC into nasal mucosa can be enhanced by forming
liposome. This research has the aim to prepare and characterize iposome laoding OXC. The OXC
liposome formula was composed by using soya lechitin and cholesterol with various amount using
thin film hydration method. Characterization by determining the encapsulation efficiency (%EE), pH,
viscosity, particle size, polydispersity of index, zeta potential, and in vitro release. The liposome of
OXC was also analyzed for its stability based on heating-coling cycle method. The proportion of best
formula was obtained at the amount of cholesterol of 42,11 mg yield %EE of 92,63%, pH of 8,47,
viscosity of 1,10 cP, and decreased amount of OXC in stability test of 0,34%. The results of particle
diameter were 579 nm, polydispersity index (PDI) of 0,34, and zeta potential of -99,38 mV. The in vitro
release of the liposome of OXC was studied and compared with OXC. The result of in vitro release
liposome OXC (F2) ahowed increase (62,26%) than (41,97%).


Kata Kunci


liposome, oxcarbazepine, cholesterol, PDI, encapsulation.

Teks Lengkap:

PDF

Referensi


Brodie MJ, French JA. Management

of epilepsy in adolescents and adults.

Handbook of Pharmacology: A

Pathophysiology approach 7th Edition,

McGrawa-Hill, USA. 2000.

Shorvon S. Oxcarbazepine: a Review,

Seizure, 9:75-79.2000

Douroumis D, Fahr A. Nano and microparticulate

formulations of poorly water

soluble drugs by using a novel optimized

technique. Eur J Pharm Bipharm, 63:173-

2016.

Shukla JB, Patel SJ. Formulation and

evaluation of self micro emulsifying

system candesartan cilexetil. Int J Pharm

Sci, 2(4): 2-5. 2010.

Woensel MV, Wauthoz N, Rosiere

R, Amighi K, Mathieu V, Lefranc F.

Formulations for intransal delivery of

pharmacological agents to combat brain

disease: A new opportunity to tackle

GBM. Cancers Journal. 5: 1020-1048.

Parvathi M. Intranasal drug delivery to

brain: An overview. Internastional Journal

of Research Pharmacy Chem. 2(3): 889-

2012.

Ghori MU, Mahdi MH, Smith AM,

Conway BR. Nasal drug delivery

systems: An overview. American Journal

of Pharmacological Sciences. 3(5): 110-

2015

Jufri M. Liposome drug delivery system.

Pharmaceutical sciences and research.

(2); 59-68. 2012.

Eloy JO, Claro SM, Petrilli R, Barcellos

JP, Lee RJ, Marchetti JM. Liposomes

as carriers of hydrophilic small

molecule drugs: strategies to enhance

encapsulation and delivery. Colloids Surf

B: Biointerfaces. 123C: 345-363. 2014.

Khan I, Elhissi A, Shah M, Alhnan,

MA, Ahmed W. Liposome-based carrier

systems and devices used for pulmonary

drug delivery. Wooodhead Publishing

Limited, United Kingdom. 395-443. 2013

Bhuchard G. Chitosan for gene delivery.

Adv Drug Deliv Rev, 52:145-150. 2001

Sashi K, Satinder K, Bharat P. A complete

review on: Liposomes. International

Research Journal of Pharmacy. 3(7).

Yu Nie LJ, Ding H, Xie L, Li L, He B,

Wu Y, Gu Z. Cholesterol derivatives

based charged liposomes for doxorubicin

delivery: Preparation in vitro and in vivo

characterization. Theranostics, 2(11):

2012.

Shivera Du, et al. Formulation and

Evaluation of Pentoxifiline Liposome

Formulation. Digest Journal of

Nanomaterial and Biostructure. 4. 2019.

Gulati N, Nagaich U, Saraf S. Fabrication

and in vitro characterization of polymeric

nanoparticles for Parkinson’s therapy:

a novel approach. Barzilian Journal of

Pharmaceutical Sciences, 50(4): 869-

2014.

Anusha RR, Vijaykumar N, Shruthi

P. Encapsulation of emulsifying drug

delivery systems (sedds) of lercanidipine

hydrochloride into hard gelatin capsules.

International Journal of Biopharmaceutics,

(2): 73-82. 2014.

Aremu OI, Oduyela OO. Evaluation

of metronidazole suspension. African

Journal Biochem Res, 9(12): 595-597.

Rajaran S, Natham R. Design and

characterization of asorbic acid stabilized

rifampicin nanoparticles for oral delivery.

Int J Bio and Pharm Research, 4(12):

-999. 2013.

Putra, I Gusti NS, Darijanto, Sasanti

TS, Yeyet C. Formulasi sediaan liposom

nimodipine: Studi pengaruh komposisi

lipida terhadap efisiensi inkorporasi

nimodipine dan stabilitas ukuran partikel

liposom. Acta Pharmaceutica Indonesia,

(1):18-25.2014.

Kuruvila FS, Mathew F, Kuppuswanny

S. Solid Self Nanoemulsifying

Drug Delivery System (SNEDDS)

Development, Applications, and Future

Perspective: A Review. Indo Am J Pharm

Sci. 4(3): 651-669. 2017.

Das Neves JM, Amiji M, MF Bahia,

and B. Sarmeto. Assesing the physicalchemical

properties and stability of

dapirine-loaded polymeric nanoparticles.

International Journal of Pharmacutics,

(2): 307-314. 2013




DOI: https://doi.org/10.24198/ijpst.v10i2.33707

Refbacks

  • Saat ini tidak ada refbacks.


 Switch to English

Back to Top

View My Stats

Penerbit Universitas Padjadjaran

Jurnal ini terindeks di :

      

Creative Commons Attribution :

Creative Commons License
Indonesian Journal of Pharmaceutical Science and Technology by Universitas Padjadjaran is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Based on a work at http://jurnal.unpad.ac.id/ijpst/