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
Main Authors: Milović, Mladen, Simović, Spomenka, Lošić, Dušan, Dashevskiy, Andriy, Ibrić, Svetlana
Format: Journal Article
Language:English
Published: Netherlands 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.
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
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  surname: Milović
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  givenname: Spomenka
  surname: Simović
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  email: spomenka.simovic@unisa.edu.au
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  givenname: Dušan
  surname: Lošić
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  email: dusan.losic@adelaide.edu.au
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  givenname: Andriy
  surname: Dashevskiy
  fullname: Dashevskiy, Andriy
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  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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Cites_doi 10.1021/op900133z
10.1039/f29767201525
10.1016/j.ejps.2006.04.016
10.1016/j.ejpb.2009.06.001
10.1016/S0378-5173(03)00365-X
10.1016/j.tibtech.2008.11.003
10.1023/A:1016212804288
10.1039/c0cc01305f
10.1016/j.ijpharm.2008.08.046
10.1016/j.ejpb.2006.03.011
10.1080/10717540500395007
10.1016/j.ijpharm.2004.06.021
10.1016/j.powtec.2011.04.023
10.1081/PDT-100100540
10.1016/S0939-6411(00)00076-X
10.2217/nnm.11.29
10.1016/S0378-5173(02)00003-0
10.1002/adma.200803778
10.2174/157016311796799026
10.1002/jps.21638
10.1016/j.micromeso.2008.07.002
10.1016/j.jcis.2008.10.077
10.1016/0005-2736(94)90337-9
10.1002/jps.10455
10.1016/j.ijpharm.2011.04.015
10.1016/j.jconrel.2009.07.014
10.1081/PDT-120002234
10.1002/anie.200604488
10.1021/la102083t
10.1016/j.addr.2007.09.006
10.1016/j.addr.2007.10.010
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Keywords Labrasol
Lecithin
Diatoms
Carbamazepine
Solid self-emulsifying phospholipid suspension
Language English
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References Prajapati, Pate (b0150) 2007; 1
Arien, Henry-Toulme, Dupuy (b0015) 1994; 1193
Sinn Aw, Simovic, Yu, Addai-Mensah, Losic (b0170) 2011; 6
Nicolaos, Crauste-Manciet, Farinotti, Brossard (b0130) 2003; 263
Shanmugam, Park, Kim, Piao, Yong, Choi, Woo (b0155) 2011; 412
Levy, Wilensky, Anderson (b0105) 1992
Gua, Lib, Gandhia, Raghavana (b0070) 2004; 283
Amidon, Lennernas, Shah, Crison (b0010) 1995; 12
Simovic, Eskandar, Sinn Aw, Losic, Prestige (b0160) 2011; 8
Losic, Mitchell, Voelcker (b0115) 2009; 21
Speybroeck, Barillaro, Do Thi, Mellaerts, Martens, Humbeeck, Vermant, Annaert, Van den Mooter (b0180) 2009; 98
FDA, 1997a. Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms. Center for Drug Evaluation and Research, Rockville, MD.
CFR, 2011. Code of Federal Regulations. Part 184 – Direct Food substances affirmed as Generally Recognized as Safe. Subpart B – Listing of specific substances Affirmed as GRAS, Section 184.1400, 21CFR184.1400, p. 3.
Chakraborty, Shukla, Mishra, Singh (b0025) 2009; 73
Zhou, Labuza (b0215) 2011
Pouton, Porter (b0145) 2008; 60
Kelly, Rodrıguez-Hornedo (b0085) 2009; 13
Losic, Yu, Sin Aw, Simovic, Tierry, Addai-Mensah (b0120) 2010; 46
Kumeria, Bariana, Altalhi, Kurkuri, Gibson, Yang, Losic (b0095) 2013; 1
Wang (b0190) 2009; 117
Agarwal, Siddiqui, Ali, Nazzal (b0005) 2009; 366
European Pharmacopeia, 2008. 6th ed., European Department for the Quality of Medicines, Strasburg, pp. 1411–1412 (Supplement 2008).
Gordon, Losic, Tiffany, Nagy, Sterrenburg (b0060) 2009; 27
Florence, Attwood (b0050) 2006
Wang, Dong, Eastoe, Li (b0195) 2009; 330
Sinn Aw, Simovic, Yu, Addai-Mensah, Losic (b0165) 2012; 223
FDA, 1995. Guidance for Industry: Immediate Release Solid Oral Dosage Forms – Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing, and In Vivo Bioequivalance Documentation. Center for Drug Evaluation and Research, Rockville, MD.
Israelachvili, Mitchell, Ninham (b0075) 1976; 72
Li, Han, Zhang, Grant, Saryanarajanan (b0110) 2000; 5
Pouton (b0140) 2006; 29
Snow, Allen, Ennis, Litster (b0175) 1997
Goodman, Gilman, Hardman, Limbird (b0055) 2001
Yoshihashi, Yonemochi, Terada (b0205) 2002; 7
Jannin, Musakhanian, Marchaud (b0080) 2008; 60
Xu, He, Nie, Guan, Zhang, Yang (b0200) 2009; 140
Grzesiak, Lang, Kim, Matzeger (b0065) 2003; 92
Nazzal, Smalyukh, Lavrentovich, Khan (b0125) 2002; 235
Yu, Addai-Mensah, Losic (b0210) 2010; 26
FDA, 1997b. Guidance for Industry: SUPAC-MR: Modified Release Solid Oral Dosage Forms – Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing, and In Vivo Bioequivalance Documentation. Center for Drug Evaluation and Research, Rockville, MD.
Leuner, Dressman (b0100) 2000; 50
Koga, Kusawake, Ito, Sugioka, Shibata, Takada (b0090) 2006; 64
Potluri, Betageri (b0135) 2006; 13
Valet-Regi, Balas, Arcos (b0185) 2007; 46
Grzesiak (10.1016/j.ejps.2014.07.010_b0065) 2003; 92
Sinn Aw (10.1016/j.ejps.2014.07.010_b0170) 2011; 6
Potluri (10.1016/j.ejps.2014.07.010_b0135) 2006; 13
Wang (10.1016/j.ejps.2014.07.010_b0190) 2009; 117
Li (10.1016/j.ejps.2014.07.010_b0110) 2000; 5
Florence (10.1016/j.ejps.2014.07.010_b0050) 2006
Pouton (10.1016/j.ejps.2014.07.010_b0140) 2006; 29
10.1016/j.ejps.2014.07.010_b0040
Losic (10.1016/j.ejps.2014.07.010_b0120) 2010; 46
Losic (10.1016/j.ejps.2014.07.010_b0115) 2009; 21
Shanmugam (10.1016/j.ejps.2014.07.010_b0155) 2011; 412
Xu (10.1016/j.ejps.2014.07.010_b0200) 2009; 140
Levy (10.1016/j.ejps.2014.07.010_b0105) 1992
10.1016/j.ejps.2014.07.010_b0045
Snow (10.1016/j.ejps.2014.07.010_b0175) 1997
Speybroeck (10.1016/j.ejps.2014.07.010_b0180) 2009; 98
10.1016/j.ejps.2014.07.010_b0020
Prajapati (10.1016/j.ejps.2014.07.010_b0150) 2007; 1
Leuner (10.1016/j.ejps.2014.07.010_b0100) 2000; 50
Nicolaos (10.1016/j.ejps.2014.07.010_b0130) 2003; 263
Yu (10.1016/j.ejps.2014.07.010_b0210) 2010; 26
Valet-Regi (10.1016/j.ejps.2014.07.010_b0185) 2007; 46
Arien (10.1016/j.ejps.2014.07.010_b0015) 1994; 1193
Jannin (10.1016/j.ejps.2014.07.010_b0080) 2008; 60
Amidon (10.1016/j.ejps.2014.07.010_b0010) 1995; 12
Pouton (10.1016/j.ejps.2014.07.010_b0145) 2008; 60
Wang (10.1016/j.ejps.2014.07.010_b0195) 2009; 330
Sinn Aw (10.1016/j.ejps.2014.07.010_b0165) 2012; 223
10.1016/j.ejps.2014.07.010_b0030
Yoshihashi (10.1016/j.ejps.2014.07.010_b0205) 2002; 7
Chakraborty (10.1016/j.ejps.2014.07.010_b0025) 2009; 73
Nazzal (10.1016/j.ejps.2014.07.010_b0125) 2002; 235
Gua (10.1016/j.ejps.2014.07.010_b0070) 2004; 283
Agarwal (10.1016/j.ejps.2014.07.010_b0005) 2009; 366
Kumeria (10.1016/j.ejps.2014.07.010_b0095) 2013; 1
Koga (10.1016/j.ejps.2014.07.010_b0090) 2006; 64
Simovic (10.1016/j.ejps.2014.07.010_b0160) 2011; 8
10.1016/j.ejps.2014.07.010_b0035
Goodman (10.1016/j.ejps.2014.07.010_b0055) 2001
Israelachvili (10.1016/j.ejps.2014.07.010_b0075) 1976; 72
Kelly (10.1016/j.ejps.2014.07.010_b0085) 2009; 13
Gordon (10.1016/j.ejps.2014.07.010_b0060) 2009; 27
Zhou (10.1016/j.ejps.2014.07.010_b0215) 2011
References_xml – volume: 73
  start-page: 1
  year: 2009
  end-page: 15
  ident: b0025
  article-title: Lipid – an emerging platform for oral delivery of drugs with poor bioavailability review article
  publication-title: Eur. J. Pharm. Biopharm.
  contributor:
    fullname: Singh
– volume: 46
  start-page: 7548
  year: 2007
  end-page: 7558
  ident: b0185
  article-title: Mesoporous materials for drug delivery
  publication-title: Angew. Chem. Int. Ed.
  contributor:
    fullname: Arcos
– volume: 21
  start-page: 2947
  year: 2009
  end-page: 2958
  ident: b0115
  article-title: Diatomaceous lessons in nanotechnology and advanced materials
  publication-title: Adv. Mater.
  contributor:
    fullname: Voelcker
– volume: 72
  start-page: 1525
  year: 1976
  end-page: 1568
  ident: b0075
  article-title: Theory of self-assembly of hydrocarbon amphiphiles into micelles and bilayers
  publication-title: J. Chem. Soc. Faraday Trans. II
  contributor:
    fullname: Ninham
– year: 2006
  ident: b0050
  article-title: Physicochemical Principles of Pharmacy
  contributor:
    fullname: Attwood
– volume: 140
  start-page: 61
  year: 2009
  end-page: 68
  ident: b0200
  article-title: Optimized preparation of vinpocetine proliposomes by a novel method and in vivo evaluation of its pharmacokinetics in New Zealand rabbits
  publication-title: J. Control. Rel.
  contributor:
    fullname: Yang
– volume: 7
  start-page: 89
  year: 2002
  end-page: 95
  ident: b0205
  article-title: Estimation of initial dissolution rate of drug substance by thermal analysis: application for carbamazepine
  publication-title: Pharm. Dev. Technol.
  contributor:
    fullname: Terada
– volume: 13
  start-page: 1291
  year: 2009
  end-page: 1300
  ident: b0085
  article-title: Solvent effects on the crystallization and preferential nucleation of carbamazepine anhydrous polymorphs: a molecular recognition perspective
  publication-title: Organic Process Res. Develop.
  contributor:
    fullname: Rodrıguez-Hornedo
– volume: 26
  start-page: 14068
  year: 2010
  end-page: 14072
  ident: b0210
  article-title: Synthesis of self-supporting gold microstructures with 3-d morphologies by direct replication of diatom templates
  publication-title: Langmuir
  contributor:
    fullname: Losic
– year: 2001
  ident: b0055
  article-title: Goodman & Gilman’s the pharmacological basis of therapeutics
  contributor:
    fullname: Limbird
– volume: 98
  start-page: 2648
  year: 2009
  end-page: 2658
  ident: b0180
  article-title: Ordered mesoporous silica material SBA-15: a broad-spectrum formulation platform for poorly soluble drugs
  publication-title: J. Pharm. Sci.
  contributor:
    fullname: Van den Mooter
– volume: 27
  start-page: 116
  year: 2009
  end-page: 127
  ident: b0060
  article-title: The glass menagerie: diatoms for novel applications in nanotechnology
  publication-title: Trends Biotechnol.
  contributor:
    fullname: Sterrenburg
– start-page: 1
  year: 1992
  end-page: 29
  ident: b0105
  article-title: Carbamazepine, valproic acid, phenobarbital, and ethosuximide
  publication-title: Applied Pharmacokinetics. Principles of Therapeutic Drug Monitoring. Applied Therapeutics
  contributor:
    fullname: Anderson
– volume: 6
  start-page: 1159
  year: 2011
  end-page: 1173
  ident: b0170
  article-title: Silica microcapsules from diatoms as a new carrier for delivery of therapeutics
  publication-title: Nanomedicine
  contributor:
    fullname: Losic
– volume: 330
  start-page: 443
  year: 2009
  end-page: 448
  ident: b0195
  article-title: Design and optimization of a new self-nanoemulsifying drug delivery system
  publication-title: J. Colloid Interface Sci.
  contributor:
    fullname: Li
– volume: 117
  start-page: 1
  year: 2009
  end-page: 9
  ident: b0190
  article-title: Ordered mesoporous materials for drug delivery
  publication-title: Micropor. Mesopor. Mat
  contributor:
    fullname: Wang
– volume: 64
  start-page: 82
  year: 2006
  end-page: 91
  ident: b0090
  article-title: Enhancing mechanism of Labrasol on intestinal membrane permeability of the hydrophilic drug gentamicin sulfate
  publication-title: Eur. J. Pharm. Biopharm.
  contributor:
    fullname: Takada
– volume: 46
  start-page: 6323
  year: 2010
  end-page: 6325
  ident: b0120
  article-title: Surface functionalization of diatoms with dopamine modified iron oxide nanoparticles: toward magnetically guided drug microcarriers with biologically derived morphologies
  publication-title: Chem. Commun.
  contributor:
    fullname: Addai-Mensah
– volume: 223
  start-page: 52
  year: 2012
  end-page: 58
  ident: b0165
  article-title: Porous silica microshells from diatoms as biocarrier for drug delivery applications
  publication-title: Powder Technol.
  contributor:
    fullname: Losic
– volume: 283
  start-page: 117
  year: 2004
  end-page: 125
  ident: b0070
  article-title: Grouping solvents by statistical analysis of solvent property parameters: implication to polymorph screening
  publication-title: Int. J. Pharm.
  contributor:
    fullname: Raghavana
– volume: 60
  start-page: 734
  year: 2008
  end-page: 746
  ident: b0080
  article-title: Approaches for the development of solid and semi-solid lipid-based formulations
  publication-title: Adv. Drug Deliver
  contributor:
    fullname: Marchaud
– volume: 235
  start-page: 247
  year: 2002
  end-page: 265
  ident: b0125
  article-title: Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation
  publication-title: Int. J. Pharm.
  contributor:
    fullname: Khan
– volume: 412
  start-page: 99
  year: 2011
  end-page: 105
  ident: b0155
  article-title: Enhanced bioavailability and retinal accumulation of lutein from self-emulsifying phospholipid suspension (SEPS)
  publication-title: Int. J. Pharm
  contributor:
    fullname: Woo
– volume: 60
  start-page: 625
  year: 2008
  end-page: 637
  ident: b0145
  article-title: Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies
  publication-title: Adv. Drug Deliver. Rev.
  contributor:
    fullname: Porter
– volume: 50
  start-page: 47
  year: 2000
  end-page: 60
  ident: b0100
  article-title: Improving drug solubility for oral delivery using solid dispersions
  publication-title: Eur. J. Pharm. Biopharm
  contributor:
    fullname: Dressman
– volume: 1
  start-page: 1
  year: 2007
  end-page: 8
  ident: b0150
  article-title: Conventional and alternative methods to improve oral bioavailability of lipophilic drugs
  publication-title: Asian J. Pharm.
  contributor:
    fullname: Pate
– volume: 366
  start-page: 44
  year: 2009
  end-page: 52
  ident: b0005
  article-title: Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS)
  publication-title: Int. J. Pharm.
  contributor:
    fullname: Nazzal
– volume: 92
  start-page: 2260
  year: 2003
  end-page: 2271
  ident: b0065
  article-title: Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I
  publication-title: J. Pharm. Sci.
  contributor:
    fullname: Matzeger
– volume: 1
  start-page: 6302
  year: 2013
  end-page: 6311
  ident: b0095
  article-title: Graphene oxide decorated diatom silica particles as a new nano-hybrid: towards smart natural drug microcarriers
  publication-title: J. Mater. Chem.
  contributor:
    fullname: Losic
– volume: 8
  start-page: 250
  year: 2011
  end-page: 268
  ident: b0160
  article-title: Silica materials in drug delivery applications
  publication-title: Curr. Drug Discov. Technol.
  contributor:
    fullname: Prestige
– volume: 5
  start-page: 257
  year: 2000
  end-page: 266
  ident: b0110
  article-title: In situ dehydration of CBZ dihydrate: a novel technique to prepare amorphous anhydrous carbamazepine
  publication-title: Pharm. Dev. Tech.
  contributor:
    fullname: Saryanarajanan
– year: 2011
  ident: b0215
  article-title: Encyclopedia of Dairy Sciences
  contributor:
    fullname: Labuza
– volume: 1193
  start-page: 93
  year: 1994
  end-page: 100
  ident: b0015
  article-title: Calcitonin loaded liposomes: stability under acidic conditions and bile salts-induced disruption resulting in calcitonin–phospholipid complex formation
  publication-title: Biochim. Biophys. Acta
  contributor:
    fullname: Dupuy
– volume: 263
  start-page: 165
  year: 2003
  end-page: 171
  ident: b0130
  article-title: Improvement of cefpodoxime proxetil oral absorption in rats by an oil-in water submicron emulsion
  publication-title: Int. J. Pharm.
  contributor:
    fullname: Brossard
– start-page: 8
  year: 1997
  ident: b0175
  article-title: Size reduction and size enlargement
  publication-title: Perry’s Chemical Engineers’ Handbook
  contributor:
    fullname: Litster
– volume: 12
  start-page: 413
  year: 1995
  ident: b0010
  article-title: A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
  publication-title: Pharm. Res.
  contributor:
    fullname: Crison
– volume: 13
  start-page: 227
  year: 2006
  end-page: 232
  ident: b0135
  article-title: Mixed-micellar proliposomal systems for enhanced oral delivery of progesterone
  publication-title: Drug Deliver.
  contributor:
    fullname: Betageri
– volume: 29
  start-page: 278
  year: 2006
  end-page: 287
  ident: b0140
  article-title: Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system
  publication-title: Eur. J. Pharm. Sci.
  contributor:
    fullname: Pouton
– ident: 10.1016/j.ejps.2014.07.010_b0045
– volume: 1
  start-page: 1
  year: 2007
  ident: 10.1016/j.ejps.2014.07.010_b0150
  article-title: Conventional and alternative methods to improve oral bioavailability of lipophilic drugs
  publication-title: Asian J. Pharm.
  contributor:
    fullname: Prajapati
– volume: 13
  start-page: 1291
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0085
  article-title: Solvent effects on the crystallization and preferential nucleation of carbamazepine anhydrous polymorphs: a molecular recognition perspective
  publication-title: Organic Process Res. Develop.
  doi: 10.1021/op900133z
  contributor:
    fullname: Kelly
– volume: 72
  start-page: 1525
  year: 1976
  ident: 10.1016/j.ejps.2014.07.010_b0075
  article-title: Theory of self-assembly of hydrocarbon amphiphiles into micelles and bilayers
  publication-title: J. Chem. Soc. Faraday Trans. II
  doi: 10.1039/f29767201525
  contributor:
    fullname: Israelachvili
– volume: 29
  start-page: 278
  year: 2006
  ident: 10.1016/j.ejps.2014.07.010_b0140
  article-title: Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system
  publication-title: Eur. J. Pharm. Sci.
  doi: 10.1016/j.ejps.2006.04.016
  contributor:
    fullname: Pouton
– ident: 10.1016/j.ejps.2014.07.010_b0020
– volume: 73
  start-page: 1
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0025
  article-title: Lipid – an emerging platform for oral delivery of drugs with poor bioavailability review article
  publication-title: Eur. J. Pharm. Biopharm.
  doi: 10.1016/j.ejpb.2009.06.001
  contributor:
    fullname: Chakraborty
– volume: 263
  start-page: 165
  year: 2003
  ident: 10.1016/j.ejps.2014.07.010_b0130
  article-title: Improvement of cefpodoxime proxetil oral absorption in rats by an oil-in water submicron emulsion
  publication-title: Int. J. Pharm.
  doi: 10.1016/S0378-5173(03)00365-X
  contributor:
    fullname: Nicolaos
– volume: 27
  start-page: 116
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0060
  article-title: The glass menagerie: diatoms for novel applications in nanotechnology
  publication-title: Trends Biotechnol.
  doi: 10.1016/j.tibtech.2008.11.003
  contributor:
    fullname: Gordon
– volume: 12
  start-page: 413
  year: 1995
  ident: 10.1016/j.ejps.2014.07.010_b0010
  article-title: A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
  publication-title: Pharm. Res.
  doi: 10.1023/A:1016212804288
  contributor:
    fullname: Amidon
– year: 2001
  ident: 10.1016/j.ejps.2014.07.010_b0055
  contributor:
    fullname: Goodman
– volume: 46
  start-page: 6323
  year: 2010
  ident: 10.1016/j.ejps.2014.07.010_b0120
  article-title: Surface functionalization of diatoms with dopamine modified iron oxide nanoparticles: toward magnetically guided drug microcarriers with biologically derived morphologies
  publication-title: Chem. Commun.
  doi: 10.1039/c0cc01305f
  contributor:
    fullname: Losic
– start-page: 1
  year: 1992
  ident: 10.1016/j.ejps.2014.07.010_b0105
  article-title: Carbamazepine, valproic acid, phenobarbital, and ethosuximide
  contributor:
    fullname: Levy
– volume: 366
  start-page: 44
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0005
  article-title: Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS)
  publication-title: Int. J. Pharm.
  doi: 10.1016/j.ijpharm.2008.08.046
  contributor:
    fullname: Agarwal
– volume: 64
  start-page: 82
  year: 2006
  ident: 10.1016/j.ejps.2014.07.010_b0090
  article-title: Enhancing mechanism of Labrasol on intestinal membrane permeability of the hydrophilic drug gentamicin sulfate
  publication-title: Eur. J. Pharm. Biopharm.
  doi: 10.1016/j.ejpb.2006.03.011
  contributor:
    fullname: Koga
– volume: 13
  start-page: 227
  year: 2006
  ident: 10.1016/j.ejps.2014.07.010_b0135
  article-title: Mixed-micellar proliposomal systems for enhanced oral delivery of progesterone
  publication-title: Drug Deliver.
  doi: 10.1080/10717540500395007
  contributor:
    fullname: Potluri
– ident: 10.1016/j.ejps.2014.07.010_b0035
– year: 2011
  ident: 10.1016/j.ejps.2014.07.010_b0215
  contributor:
    fullname: Zhou
– volume: 283
  start-page: 117
  year: 2004
  ident: 10.1016/j.ejps.2014.07.010_b0070
  article-title: Grouping solvents by statistical analysis of solvent property parameters: implication to polymorph screening
  publication-title: Int. J. Pharm.
  doi: 10.1016/j.ijpharm.2004.06.021
  contributor:
    fullname: Gua
– volume: 223
  start-page: 52
  year: 2012
  ident: 10.1016/j.ejps.2014.07.010_b0165
  article-title: Porous silica microshells from diatoms as biocarrier for drug delivery applications
  publication-title: Powder Technol.
  doi: 10.1016/j.powtec.2011.04.023
  contributor:
    fullname: Sinn Aw
– volume: 5
  start-page: 257
  issue: 2
  year: 2000
  ident: 10.1016/j.ejps.2014.07.010_b0110
  article-title: In situ dehydration of CBZ dihydrate: a novel technique to prepare amorphous anhydrous carbamazepine
  publication-title: Pharm. Dev. Tech.
  doi: 10.1081/PDT-100100540
  contributor:
    fullname: Li
– volume: 50
  start-page: 47
  year: 2000
  ident: 10.1016/j.ejps.2014.07.010_b0100
  article-title: Improving drug solubility for oral delivery using solid dispersions
  publication-title: Eur. J. Pharm. Biopharm.
  doi: 10.1016/S0939-6411(00)00076-X
  contributor:
    fullname: Leuner
– volume: 6
  start-page: 1159
  issue: 7
  year: 2011
  ident: 10.1016/j.ejps.2014.07.010_b0170
  article-title: Silica microcapsules from diatoms as a new carrier for delivery of therapeutics
  publication-title: Nanomedicine
  doi: 10.2217/nnm.11.29
  contributor:
    fullname: Sinn Aw
– volume: 235
  start-page: 247
  year: 2002
  ident: 10.1016/j.ejps.2014.07.010_b0125
  article-title: Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation
  publication-title: Int. J. Pharm.
  doi: 10.1016/S0378-5173(02)00003-0
  contributor:
    fullname: Nazzal
– volume: 1
  start-page: 6302
  year: 2013
  ident: 10.1016/j.ejps.2014.07.010_b0095
  article-title: Graphene oxide decorated diatom silica particles as a new nano-hybrid: towards smart natural drug microcarriers
  publication-title: J. Mater. Chem.
  contributor:
    fullname: Kumeria
– volume: 21
  start-page: 2947
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0115
  article-title: Diatomaceous lessons in nanotechnology and advanced materials
  publication-title: Adv. Mater.
  doi: 10.1002/adma.200803778
  contributor:
    fullname: Losic
– volume: 8
  start-page: 250
  issue: 3
  year: 2011
  ident: 10.1016/j.ejps.2014.07.010_b0160
  article-title: Silica materials in drug delivery applications
  publication-title: Curr. Drug Discov. Technol.
  doi: 10.2174/157016311796799026
  contributor:
    fullname: Simovic
– start-page: 8
  year: 1997
  ident: 10.1016/j.ejps.2014.07.010_b0175
  article-title: Size reduction and size enlargement
  contributor:
    fullname: Snow
– volume: 98
  start-page: 2648
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0180
  article-title: Ordered mesoporous silica material SBA-15: a broad-spectrum formulation platform for poorly soluble drugs
  publication-title: J. Pharm. Sci.
  doi: 10.1002/jps.21638
  contributor:
    fullname: Speybroeck
– volume: 117
  start-page: 1
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0190
  article-title: Ordered mesoporous materials for drug delivery
  publication-title: Micropor. Mesopor. Mat.
  doi: 10.1016/j.micromeso.2008.07.002
  contributor:
    fullname: Wang
– volume: 330
  start-page: 443
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0195
  article-title: Design and optimization of a new self-nanoemulsifying drug delivery system
  publication-title: J. Colloid Interface Sci.
  doi: 10.1016/j.jcis.2008.10.077
  contributor:
    fullname: Wang
– volume: 1193
  start-page: 93
  year: 1994
  ident: 10.1016/j.ejps.2014.07.010_b0015
  article-title: Calcitonin loaded liposomes: stability under acidic conditions and bile salts-induced disruption resulting in calcitonin–phospholipid complex formation
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/0005-2736(94)90337-9
  contributor:
    fullname: Arien
– ident: 10.1016/j.ejps.2014.07.010_b0040
– volume: 92
  start-page: 2260
  year: 2003
  ident: 10.1016/j.ejps.2014.07.010_b0065
  article-title: Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I
  publication-title: J. Pharm. Sci.
  doi: 10.1002/jps.10455
  contributor:
    fullname: Grzesiak
– volume: 412
  start-page: 99
  year: 2011
  ident: 10.1016/j.ejps.2014.07.010_b0155
  article-title: Enhanced bioavailability and retinal accumulation of lutein from self-emulsifying phospholipid suspension (SEPS)
  publication-title: Int. J. Pharm.
  doi: 10.1016/j.ijpharm.2011.04.015
  contributor:
    fullname: Shanmugam
– volume: 140
  start-page: 61
  year: 2009
  ident: 10.1016/j.ejps.2014.07.010_b0200
  article-title: Optimized preparation of vinpocetine proliposomes by a novel method and in vivo evaluation of its pharmacokinetics in New Zealand rabbits
  publication-title: J. Control. Rel.
  doi: 10.1016/j.jconrel.2009.07.014
  contributor:
    fullname: Xu
– volume: 7
  start-page: 89
  issue: 1
  year: 2002
  ident: 10.1016/j.ejps.2014.07.010_b0205
  article-title: Estimation of initial dissolution rate of drug substance by thermal analysis: application for carbamazepine
  publication-title: Pharm. Dev. Technol.
  doi: 10.1081/PDT-120002234
  contributor:
    fullname: Yoshihashi
– volume: 46
  start-page: 7548
  issue: 40
  year: 2007
  ident: 10.1016/j.ejps.2014.07.010_b0185
  article-title: Mesoporous materials for drug delivery
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.200604488
  contributor:
    fullname: Valet-Regi
– ident: 10.1016/j.ejps.2014.07.010_b0030
– volume: 26
  start-page: 14068
  year: 2010
  ident: 10.1016/j.ejps.2014.07.010_b0210
  article-title: Synthesis of self-supporting gold microstructures with 3-d morphologies by direct replication of diatom templates
  publication-title: Langmuir
  doi: 10.1021/la102083t
  contributor:
    fullname: Yu
– year: 2006
  ident: 10.1016/j.ejps.2014.07.010_b0050
  contributor:
    fullname: Florence
– volume: 60
  start-page: 734
  year: 2008
  ident: 10.1016/j.ejps.2014.07.010_b0080
  article-title: Approaches for the development of solid and semi-solid lipid-based formulations
  publication-title: Adv. Drug Deliver. Rev.
  doi: 10.1016/j.addr.2007.09.006
  contributor:
    fullname: Jannin
– volume: 60
  start-page: 625
  year: 2008
  ident: 10.1016/j.ejps.2014.07.010_b0145
  article-title: Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies
  publication-title: Adv. Drug Deliver. Rev.
  doi: 10.1016/j.addr.2007.10.010
  contributor:
    fullname: Pouton
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Snippet [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...
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
URI https://dx.doi.org/10.1016/j.ejps.2014.07.010
https://www.ncbi.nlm.nih.gov/pubmed/25125211
https://search.proquest.com/docview/1562661261
Volume 63
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