Solid self-emulsifying phospholipid suspension (SSEPS) with diatom as a drug carrier
[Display omitted] We report the application of diatom as a solid carrier for water insoluble drugs applied in oral drug delivery system based on the self-emulsifying drug delivery system (SEDDS) caprylocaproyl macrogol-8 glycerides/lecithin/propylene glycol/caprylic/capric triglyceride. Diatoms are...
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Published in: | European journal of pharmaceutical sciences Vol. 63; pp. 226 - 232 |
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Elsevier B.V
15-10-2014
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Abstract | [Display omitted]
We report the application of diatom as a solid carrier for water insoluble drugs applied in oral drug delivery system based on the self-emulsifying drug delivery system (SEDDS) caprylocaproyl macrogol-8 glycerides/lecithin/propylene glycol/caprylic/capric triglyceride. Diatoms are fossilized skeletons of photosynthetic algae with complex 3-dimensional (3D), porous structure consisting of amorphous silica, obtained by purification of diatomaceous earth. Different solid samples of carbamazepine (CBZ) suspension in SEDDS, called solid self-emulsifying phospholipid suspension (SSEPS), were prepared using two methods: adsorption of CBZ dispersion in SEDDS by gentle mixing with diatoms in mortar with pestle (Method A) or dispersion of diatoms in ethanol solution of CBZ and SEDDS components, followed by ethanol evaporation (Method B). Release rate of CBZ from SSEPS was significantly higher in comparison to pure drug, physical mixture of diatoms and CBZ as well as solid dispersion of pure CBZ and diatoms obtained by ethanol evaporation. The dissolution of CBZ from SSEPS sample prepared using method B was faster than from the sample prepared by the method A. Higher dissolution for sample prepared by the method B can be attributed to the partial adsorption (deeper localization) of liquid material inside the pores of diatoms. Upon storage of the samples under accelerated conditions (40°C and 70% RH) for 10weeks no significant changes in CBZ crystallinity and dissolution was in case of SSEPS, contrary to solid dispersion with increased crystallinity, indicating that diatoms with adsorbed liquid CBZ-loaded SEPS can maintain initial CBZ characteristics. |
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AbstractList | [Display omitted]
We report the application of diatom as a solid carrier for water insoluble drugs applied in oral drug delivery system based on the self-emulsifying drug delivery system (SEDDS) caprylocaproyl macrogol-8 glycerides/lecithin/propylene glycol/caprylic/capric triglyceride. Diatoms are fossilized skeletons of photosynthetic algae with complex 3-dimensional (3D), porous structure consisting of amorphous silica, obtained by purification of diatomaceous earth. Different solid samples of carbamazepine (CBZ) suspension in SEDDS, called solid self-emulsifying phospholipid suspension (SSEPS), were prepared using two methods: adsorption of CBZ dispersion in SEDDS by gentle mixing with diatoms in mortar with pestle (Method A) or dispersion of diatoms in ethanol solution of CBZ and SEDDS components, followed by ethanol evaporation (Method B). Release rate of CBZ from SSEPS was significantly higher in comparison to pure drug, physical mixture of diatoms and CBZ as well as solid dispersion of pure CBZ and diatoms obtained by ethanol evaporation. The dissolution of CBZ from SSEPS sample prepared using method B was faster than from the sample prepared by the method A. Higher dissolution for sample prepared by the method B can be attributed to the partial adsorption (deeper localization) of liquid material inside the pores of diatoms. Upon storage of the samples under accelerated conditions (40°C and 70% RH) for 10weeks no significant changes in CBZ crystallinity and dissolution was in case of SSEPS, contrary to solid dispersion with increased crystallinity, indicating that diatoms with adsorbed liquid CBZ-loaded SEPS can maintain initial CBZ characteristics. We report the application of diatom as a solid carrier for water insoluble drugs applied in oral drug delivery system based on the self-emulsifying drug delivery system (SEDDS) caprylocaproyl macrogol-8 glycerides/lecithin/propylene glycol/caprylic/capric triglyceride. Diatoms are fossilized skeletons of photosynthetic algae with complex 3-dimensional (3D), porous structure consisting of amorphous silica, obtained by purification of diatomaceous earth. Different solid samples of carbamazepine (CBZ) suspension in SEDDS, called solid self-emulsifying phospholipid suspension (SSEPS), were prepared using two methods: adsorption of CBZ dispersion in SEDDS by gentle mixing with diatoms in mortar with pestle (Method A) or dispersion of diatoms in ethanol solution of CBZ and SEDDS components, followed by ethanol evaporation (Method B). Release rate of CBZ from SSEPS was significantly higher in comparison to pure drug, physical mixture of diatoms and CBZ as well as solid dispersion of pure CBZ and diatoms obtained by ethanol evaporation. The dissolution of CBZ from SSEPS sample prepared using method B was faster than from the sample prepared by the method A. Higher dissolution for sample prepared by the method B can be attributed to the partial adsorption (deeper localization) of liquid material inside the pores of diatoms. Upon storage of the samples under accelerated conditions (40°C and 70% RH) for 10 weeks no significant changes in CBZ crystallinity and dissolution was in case of SSEPS, contrary to solid dispersion with increased crystallinity, indicating that diatoms with adsorbed liquid CBZ-loaded SEPS can maintain initial CBZ characteristics. |
Author | Dashevskiy, Andriy Ibrić, Svetlana Lošić, Dušan Milović, Mladen Simović, Spomenka |
Author_xml | – sequence: 1 givenname: Mladen surname: Milović fullname: Milović, Mladen email: mladendbz@yahoo.com organization: University of Belgrade, Faculty of Pharmacy, Vojvode Stepe 450, 11221 Belgrade, Serbia – sequence: 2 givenname: Spomenka surname: Simović fullname: Simović, Spomenka email: spomenka.simovic@unisa.edu.au organization: University of South Australia, Ian Wark Research Institute, Mawson lakes, Adelaide, SA 5095, Australia – sequence: 3 givenname: Dušan surname: Lošić fullname: Lošić, Dušan email: dusan.losic@adelaide.edu.au organization: University of Adelaide, School of Chemical Engineering, Adelaide, SA 5005, Australia – sequence: 4 givenname: Andriy surname: Dashevskiy fullname: Dashevskiy, Andriy email: dashevsk@zedat.fu-berlin.de organization: Freie Universität Berlin, Institut für Pharmazie, Kelchstrasse 31, 12169 Berlin, Germany – sequence: 5 givenname: Svetlana surname: Ibrić fullname: Ibrić, Svetlana email: ibric@pharmacy.bg.ac.rs, svetlana.ibric@pharmacy.bg.ac.rs, ibric@beotel.net organization: University of Belgrade, Faculty of Pharmacy, Vojvode Stepe 450, 11221 Belgrade, Serbia |
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Keywords | Labrasol Lecithin Diatoms Carbamazepine Solid self-emulsifying phospholipid suspension |
Language | English |
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We report the application of diatom as a solid carrier for water insoluble drugs applied in oral drug delivery system based on the... We report the application of diatom as a solid carrier for water insoluble drugs applied in oral drug delivery system based on the self-emulsifying drug... |
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SubjectTerms | Carbamazepine Carbamazepine - chemistry Diatoms Diatoms - chemistry Drug Carriers - chemistry Drug Delivery Systems Emulsions Labrasol Lecithin Molecular Structure Particle Size Phospholipids - chemistry Porosity Silicon Dioxide - chemistry Solid self-emulsifying phospholipid suspension Surface Properties Suspensions - chemistry |
Title | Solid self-emulsifying phospholipid suspension (SSEPS) with diatom as a drug carrier |
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