Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds
Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a pr...
Ausführliche Beschreibung
Autor*in: |
Acerbi, D. [verfasserIn] Bovis, G. [verfasserIn] Carli, F. [verfasserIn] Pasini, M. [verfasserIn] Pavesi, L. [verfasserIn] Peveri, T. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
1990 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Clinical drug investigation - Berlin [u.a.] : Springer, 1989, 2(1990), Suppl 4 vom: Jan., Seite 29-36 |
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Übergeordnetes Werk: |
volume:2 ; year:1990 ; number:Suppl 4 ; month:01 ; pages:29-36 |
Links: |
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DOI / URN: |
10.1007/BF03258224 |
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Katalog-ID: |
SPR032994958 |
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520 | |a Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. | ||
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10.1007/BF03258224 doi (DE-627)SPR032994958 (SPR)BF03258224-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Acerbi, D. verfasserin aut Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds 1990 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. Dissolution Rate (dpeaa)DE-He213 Inclusion Complex (dpeaa)DE-He213 Piroxicam (dpeaa)DE-He213 Water Contact Angle (dpeaa)DE-He213 Physical Mixture (dpeaa)DE-He213 Bovis, G. verfasserin aut Carli, F. verfasserin aut Pasini, M. verfasserin aut Pavesi, L. verfasserin aut Peveri, T. verfasserin aut Enthalten in Clinical drug investigation Berlin [u.a.] : Springer, 1989 2(1990), Suppl 4 vom: Jan., Seite 29-36 (DE-627)327645083 (DE-600)2043793-6 1179-1918 nnns volume:2 year:1990 number:Suppl 4 month:01 pages:29-36 https://dx.doi.org/10.1007/BF03258224 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_702 GBV_ILN_2190 44.40 ASE AR 2 1990 Suppl 4 01 29-36 |
spelling |
10.1007/BF03258224 doi (DE-627)SPR032994958 (SPR)BF03258224-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Acerbi, D. verfasserin aut Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds 1990 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. Dissolution Rate (dpeaa)DE-He213 Inclusion Complex (dpeaa)DE-He213 Piroxicam (dpeaa)DE-He213 Water Contact Angle (dpeaa)DE-He213 Physical Mixture (dpeaa)DE-He213 Bovis, G. verfasserin aut Carli, F. verfasserin aut Pasini, M. verfasserin aut Pavesi, L. verfasserin aut Peveri, T. verfasserin aut Enthalten in Clinical drug investigation Berlin [u.a.] : Springer, 1989 2(1990), Suppl 4 vom: Jan., Seite 29-36 (DE-627)327645083 (DE-600)2043793-6 1179-1918 nnns volume:2 year:1990 number:Suppl 4 month:01 pages:29-36 https://dx.doi.org/10.1007/BF03258224 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_702 GBV_ILN_2190 44.40 ASE AR 2 1990 Suppl 4 01 29-36 |
allfields_unstemmed |
10.1007/BF03258224 doi (DE-627)SPR032994958 (SPR)BF03258224-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Acerbi, D. verfasserin aut Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds 1990 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. Dissolution Rate (dpeaa)DE-He213 Inclusion Complex (dpeaa)DE-He213 Piroxicam (dpeaa)DE-He213 Water Contact Angle (dpeaa)DE-He213 Physical Mixture (dpeaa)DE-He213 Bovis, G. verfasserin aut Carli, F. verfasserin aut Pasini, M. verfasserin aut Pavesi, L. verfasserin aut Peveri, T. verfasserin aut Enthalten in Clinical drug investigation Berlin [u.a.] : Springer, 1989 2(1990), Suppl 4 vom: Jan., Seite 29-36 (DE-627)327645083 (DE-600)2043793-6 1179-1918 nnns volume:2 year:1990 number:Suppl 4 month:01 pages:29-36 https://dx.doi.org/10.1007/BF03258224 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_702 GBV_ILN_2190 44.40 ASE AR 2 1990 Suppl 4 01 29-36 |
allfieldsGer |
10.1007/BF03258224 doi (DE-627)SPR032994958 (SPR)BF03258224-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Acerbi, D. verfasserin aut Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds 1990 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. Dissolution Rate (dpeaa)DE-He213 Inclusion Complex (dpeaa)DE-He213 Piroxicam (dpeaa)DE-He213 Water Contact Angle (dpeaa)DE-He213 Physical Mixture (dpeaa)DE-He213 Bovis, G. verfasserin aut Carli, F. verfasserin aut Pasini, M. verfasserin aut Pavesi, L. verfasserin aut Peveri, T. verfasserin aut Enthalten in Clinical drug investigation Berlin [u.a.] : Springer, 1989 2(1990), Suppl 4 vom: Jan., Seite 29-36 (DE-627)327645083 (DE-600)2043793-6 1179-1918 nnns volume:2 year:1990 number:Suppl 4 month:01 pages:29-36 https://dx.doi.org/10.1007/BF03258224 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_702 GBV_ILN_2190 44.40 ASE AR 2 1990 Suppl 4 01 29-36 |
allfieldsSound |
10.1007/BF03258224 doi (DE-627)SPR032994958 (SPR)BF03258224-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Acerbi, D. verfasserin aut Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds 1990 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. Dissolution Rate (dpeaa)DE-He213 Inclusion Complex (dpeaa)DE-He213 Piroxicam (dpeaa)DE-He213 Water Contact Angle (dpeaa)DE-He213 Physical Mixture (dpeaa)DE-He213 Bovis, G. verfasserin aut Carli, F. verfasserin aut Pasini, M. verfasserin aut Pavesi, L. verfasserin aut Peveri, T. verfasserin aut Enthalten in Clinical drug investigation Berlin [u.a.] : Springer, 1989 2(1990), Suppl 4 vom: Jan., Seite 29-36 (DE-627)327645083 (DE-600)2043793-6 1179-1918 nnns volume:2 year:1990 number:Suppl 4 month:01 pages:29-36 https://dx.doi.org/10.1007/BF03258224 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_702 GBV_ILN_2190 44.40 ASE AR 2 1990 Suppl 4 01 29-36 |
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610 ASE 44.40 bkl Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds Dissolution Rate (dpeaa)DE-He213 Inclusion Complex (dpeaa)DE-He213 Piroxicam (dpeaa)DE-He213 Water Contact Angle (dpeaa)DE-He213 Physical Mixture (dpeaa)DE-He213 |
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Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds |
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Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds |
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Acerbi, D. |
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Clinical drug investigation |
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1990 |
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Acerbi, D. Bovis, G. Carli, F. Pasini, M. Pavesi, L. Peveri, T. |
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biopharmaceutical optimisation of β-cyclodextrin inclusion compounds |
title_auth |
Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds |
abstract |
Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. |
abstractGer |
Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. |
abstract_unstemmed |
Summary To improve the biopharmaceutical performance of the nonsteroidal anti-inflammatory drug piroxicam, inclusion compounds with β-cyclodextrin carrier have been prepared and studied for a wide range of chemical, physical and pharmaceutical properties. Three bulk products were obtained, 2 by a process of freeze-drying (preparation A/1 and preparation A/2) and changing process parameters, and 1 by spray-drying (preparation B). The objective was to obtain tablets which provide a rapid-release dosage form of piroxicam. Studies were conducted in vitro and in humans and compared tablets of the inclusion complex of piroxicam and β-cyclodextrin with marketed oral and parenteral dosage forms of piroxicam. Significant differences were found in plasma levels, maximum plasma concentration ($ C_{max} $) and area under the plasma concentration-time curve (AUC), confirming that biopharmaceutical optimisation of the complexes can be achieved, leading to an overall pattern of absorption which is better than those presented by standard, non-complexed formulations of piroxicam (capsules, and ampoules for intramuscular use). Evidence for a correlation between the 2 main physicopharmaceutical variables (solubilisation kinetics of the complex and dissolution rate of the tablet) and biopharmaceutical performances support the development of the product. |
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title_short |
Biopharmaceutical Optimisation of β-Cyclodextrin Inclusion Compounds |
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