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Injection moulded c...
Injection moulded controlled release amorphous solid dispersions: Synchronized drug and polymer release for robust performance
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- Deshmukh, Shivprasad (författare)
- AstraZeneca AB,University of Bradford
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- Paradkar, Anant (författare)
- University of Bradford
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- Abrahmsén-Alami, Susanna (författare)
- AstraZeneca AB
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- Govender, Rydvikha, 1989 (författare)
- Chalmers tekniska högskola,Chalmers University of Technology,AstraZeneca AB
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- Viridén, Anna, 1977 (författare)
- AstraZeneca AB
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- Winge, Fredrik (författare)
- AstraZeneca AB
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- Matic, Hanna, 1970 (författare)
- AstraZeneca AB
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- Booth, Jonathan (författare)
- AstraZeneca AB
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- Kelly, Adrian (författare)
- University of Bradford
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(creator_code:org_t)
- Elsevier BV, 2020
- 2020
- Engelska.
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Ingår i: International Journal of Pharmaceutics. - : Elsevier BV. - 0378-5173 .- 1873-3476. ; 575
- Relaterad länk:
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https://bradscholars...
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https://doi.org/10.1...
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https://research.cha...
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Abstract
Ämnesord
Stäng
- A study has been carried out to investigate controlled release performance of caplet shaped injection moulded (IM) amorphous solid dispersion (ASD) tablets based on the model drug AZD0837 and polyethylene oxide (PEO). The physical/chemical storage stability and release robustness of the IM tablets were characterized and compared to that of conventional extended release (ER) hydrophilic matrix tablets of the same raw materials and compositions manufactured via direct compression (DC). To gain an improved understanding of the release mechanisms, the dissolution of both the polymer and the drug were studied. Under conditions where the amount of dissolution media was limited, the controlled release ASD IM tablets demonstrated complete and synchronized release of both PEO and AZD0837 whereas the release of AZD0837 was found to be slower and incomplete from conventional direct compressed ER hydrophilic matrix tablets. The results clearly indicated that AZD0837 remained amorphous throughout the dissolution process and was maintained in a supersaturated state and hence kept stable with the aid of the polymeric carrier when released in a synchronized manner. In addition, it was found that the IM tablets were robust to variation in hydrodynamics of the dissolution environment and PEO molecular weight.
Ämnesord
- NATURVETENSKAP -- Kemi -- Polymerkemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Polymer Chemistry (hsv//eng)
- NATURVETENSKAP -- Kemi -- Annan kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Other Chemistry Topics (hsv//eng)
- TEKNIK OCH TEKNOLOGIER -- Medicinteknik -- Medicinsk material- och protesteknik (hsv//swe)
- ENGINEERING AND TECHNOLOGY -- Medical Engineering -- Medical Materials (hsv//eng)
Nyckelord
- Amorphous solid dispersion (ASD)
- Release robustness
- Injection moulding (IM)
- Controlled release
- Polymer release
- Polyethylene oxide (PEO)
- Poorly soluble drug
- Oral solid dosage (OSD)
- Hot melt extrusion (HME)
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Deshmukh, Shivpr ...
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Paradkar, Anant
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Abrahmsén-Alami, ...
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Govender, Rydvik ...
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Viridén, Anna, 1 ...
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Winge, Fredrik
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visa fler...
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Matic, Hanna, 19 ...
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Booth, Jonathan
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Kelly, Adrian
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visa färre...
- Om ämnet
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- NATURVETENSKAP
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NATURVETENSKAP
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och Kemi
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och Polymerkemi
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- NATURVETENSKAP
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NATURVETENSKAP
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och Kemi
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och Annan kemi
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- TEKNIK OCH TEKNOLOGIER
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TEKNIK OCH TEKNO ...
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och Medicinteknik
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och Medicinsk materi ...
- Artiklar i publikationen
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International Jo ...
- Av lärosätet
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Chalmers tekniska högskola