Formulation of new generation drug delivery system for dry powder inhalation.
Based on the formulation method the dry powder inhalers (DPIs) can be divided in too types: carrier-based and carrier-free drug delivery systems. The newest researches report about several high potency carrier-free formulations, where the active ingredient and the excipients are together formulated to the DPI form. However, in Hungary the commercially available DPIs are carrier-based (e.g. lactose), which means that only the mic-onized active ingredient reaches the deeper lungs, the big carrier deposits in the upper airways. The present work is about formulating a high efficacy mannitol-based Pulmonary Drug Delivery System (PDDS), which is able to delivery different types of active ingredients to the deeper lungs with higher deposition rate. The present study involves the physico-chemical and aerodynamical characterisation of mannitol-based PDDS. The results demonstrated the use of the appropriate excipients (leucine, poly-vinyl-alcohol, cyclodextrine) and solvent combination (ethanol-water) during the co-spray drying, increases the inhalation properties of the mannitol. Such carrier systems with optimized properties can increase the aerolization efficacy of the active ingredient.
Medienart: |
Artikel |
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Erscheinungsjahr: |
2016 |
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Erschienen: |
2016 |
Enthalten in: |
Zur Gesamtaufnahme - volume:86 |
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Enthalten in: |
Acta pharmaceutica Hungarica - 86(2016), 3 vom: 22., Seite 75-83 |
Sprache: |
Ungarisch |
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Weiterer Titel: |
Not available |
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Beteiligte Personen: |
Chvatal, A [VerfasserIn] |
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Themen: |
3OWL53L36A |
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Anmerkungen: |
Date Completed 02.04.2018 Date Revised 02.04.2018 published: Print Citation Status MEDLINE |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM281469334 |
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245 | 1 | 0 | |a Formulation of new generation drug delivery system for dry powder inhalation. |
246 | 3 | 3 | |a Not available |
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338 | |a Band |b nc |2 rdacarrier | ||
500 | |a Date Completed 02.04.2018 | ||
500 | |a Date Revised 02.04.2018 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Based on the formulation method the dry powder inhalers (DPIs) can be divided in too types: carrier-based and carrier-free drug delivery systems. The newest researches report about several high potency carrier-free formulations, where the active ingredient and the excipients are together formulated to the DPI form. However, in Hungary the commercially available DPIs are carrier-based (e.g. lactose), which means that only the mic-onized active ingredient reaches the deeper lungs, the big carrier deposits in the upper airways. The present work is about formulating a high efficacy mannitol-based Pulmonary Drug Delivery System (PDDS), which is able to delivery different types of active ingredients to the deeper lungs with higher deposition rate. The present study involves the physico-chemical and aerodynamical characterisation of mannitol-based PDDS. The results demonstrated the use of the appropriate excipients (leucine, poly-vinyl-alcohol, cyclodextrine) and solvent combination (ethanol-water) during the co-spray drying, increases the inhalation properties of the mannitol. Such carrier systems with optimized properties can increase the aerolization efficacy of the active ingredient | ||
650 | 4 | |a Journal Article | |
650 | 7 | |a Drug Carriers |2 NLM | |
650 | 7 | |a Excipients |2 NLM | |
650 | 7 | |a Pharmaceutical Preparations |2 NLM | |
650 | 7 | |a Mannitol |2 NLM | |
650 | 7 | |a 3OWL53L36A |2 NLM | |
700 | 1 | |a Szabo, B |e verfasserin |4 aut | |
700 | 1 | |a Szabo-Revesz, P |e verfasserin |4 aut | |
700 | 1 | |a Ambrus, R |e verfasserin |4 aut | |
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