Evaluation of critical formulation parameters in design and differentiation of self-microemulsifying drug delivery systems (SMEDDSs) for oral delivery of aciclovir
Copyright © 2015 Elsevier B.V. All rights reserved..
The study investigated the influence of formulation parameters for design of self-microemulsifying drug delivery systems (SMEDDSs) comprising oil (medium chain triglycerides) (10%), surfactant (Labrasol(®), polysorbate 20, or Kolliphor(®) RH40), cosurfactant (Plurol(®) Oleique CC 497) (q.s. ad 100%), and cosolvent (glycerol or macrogol 400) (20% or 30%), and evaluate their potential as carriers for oral delivery of a poorly permeable antivirotic aciclovir (acyclovir). The drug loading capacity of the prepared formulations ranged from 0.18-31.66 mg/ml. Among a total of 60 formulations, three formulations meet the limits for average droplet size (Z-ave) and polydispersity index (PdI) that have been set for SMEDDSs (Z-ave≤100nm, PdI<0.250) upon spontaneous dispersion in 0.1M HCl and phosphate buffer pH 7.2. SMEDDSs with the highest aciclovir loading capacity (24.06 mg/ml and 21.12 mg/ml) provided the in vitro drug release rates of 0.325 mg cm(-2)min(-1) and 0.323 mg cm(-2)min(-1), respectively, and significantly enhanced drug permeability in the parallel artificial membrane permeability assay (PAMPA), in comparison with the pure drug substance. The results revealed that development of SMEDDSs with enhanced drug loading capacity and oral delivery potential, required optimization of hydrophilic ingredients, in terms of size of hydrophilic moiety of the surfactant, surfactant-to-cosurfactant mass ratio (Km), and log P of the cosolvent.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2016 |
---|---|
Erschienen: |
2016 |
Enthalten in: |
Zur Gesamtaufnahme - volume:497 |
---|---|
Enthalten in: |
International journal of pharmaceutics - 497(2016), 1-2 vom: 30. Jan., Seite 301-11 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Janković, Jovana [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 14.10.2016 Date Revised 02.12.2018 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.ijpharm.2015.11.011 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM25504447X |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM25504447X | ||
003 | DE-627 | ||
005 | 20231224173654.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2016 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.ijpharm.2015.11.011 |2 doi | |
028 | 5 | 2 | |a pubmed24n0850.xml |
035 | |a (DE-627)NLM25504447X | ||
035 | |a (NLM)26611669 | ||
035 | |a (PII)S0378-5173(15)30358-6 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Janković, Jovana |e verfasserin |4 aut | |
245 | 1 | 0 | |a Evaluation of critical formulation parameters in design and differentiation of self-microemulsifying drug delivery systems (SMEDDSs) for oral delivery of aciclovir |
264 | 1 | |c 2016 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 14.10.2016 | ||
500 | |a Date Revised 02.12.2018 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2015 Elsevier B.V. All rights reserved. | ||
520 | |a The study investigated the influence of formulation parameters for design of self-microemulsifying drug delivery systems (SMEDDSs) comprising oil (medium chain triglycerides) (10%), surfactant (Labrasol(®), polysorbate 20, or Kolliphor(®) RH40), cosurfactant (Plurol(®) Oleique CC 497) (q.s. ad 100%), and cosolvent (glycerol or macrogol 400) (20% or 30%), and evaluate their potential as carriers for oral delivery of a poorly permeable antivirotic aciclovir (acyclovir). The drug loading capacity of the prepared formulations ranged from 0.18-31.66 mg/ml. Among a total of 60 formulations, three formulations meet the limits for average droplet size (Z-ave) and polydispersity index (PdI) that have been set for SMEDDSs (Z-ave≤100nm, PdI<0.250) upon spontaneous dispersion in 0.1M HCl and phosphate buffer pH 7.2. SMEDDSs with the highest aciclovir loading capacity (24.06 mg/ml and 21.12 mg/ml) provided the in vitro drug release rates of 0.325 mg cm(-2)min(-1) and 0.323 mg cm(-2)min(-1), respectively, and significantly enhanced drug permeability in the parallel artificial membrane permeability assay (PAMPA), in comparison with the pure drug substance. The results revealed that development of SMEDDSs with enhanced drug loading capacity and oral delivery potential, required optimization of hydrophilic ingredients, in terms of size of hydrophilic moiety of the surfactant, surfactant-to-cosurfactant mass ratio (Km), and log P of the cosolvent | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Aciclovir | |
650 | 4 | |a Acyclovir | |
650 | 4 | |a In vitro drug release | |
650 | 4 | |a Parallel artificial membrane permeability assay (PAMPA) | |
650 | 4 | |a Self-dispersing drug delivery systems | |
650 | 4 | |a Self-microemulsifying drug delivery systems (SMEDDS) | |
650 | 7 | |a Drug Carriers |2 NLM | |
650 | 7 | |a Emulsions |2 NLM | |
650 | 7 | |a Glycerides |2 NLM | |
650 | 7 | |a Polysorbates |2 NLM | |
650 | 7 | |a Surface-Active Agents |2 NLM | |
650 | 7 | |a Triglycerides |2 NLM | |
650 | 7 | |a Labrasol |2 NLM | |
650 | 7 | |a 00BT03FSO2 |2 NLM | |
650 | 7 | |a Polyethylene Glycols |2 NLM | |
650 | 7 | |a 3WJQ0SDW1A |2 NLM | |
650 | 7 | |a Acyclovir |2 NLM | |
650 | 7 | |a X4HES1O11F |2 NLM | |
700 | 1 | |a Djekic, Ljiljana |e verfasserin |4 aut | |
700 | 1 | |a Dobričić, Vladimir |e verfasserin |4 aut | |
700 | 1 | |a Primorac, Marija |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t International journal of pharmaceutics |d 1992 |g 497(2016), 1-2 vom: 30. Jan., Seite 301-11 |w (DE-627)NLM07779785X |x 1873-3476 |7 nnns |
773 | 1 | 8 | |g volume:497 |g year:2016 |g number:1-2 |g day:30 |g month:01 |g pages:301-11 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.ijpharm.2015.11.011 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 497 |j 2016 |e 1-2 |b 30 |c 01 |h 301-11 |