AbstractEven that orodispersible tablets (ODTs) have been successfully used in therapy for more than 20years, there is still no compendial method of their disintegration time evaluation other than the pharmacopoeial disintegration test conducted in 800–900mL of distilled water. Therefore, several alternative tests more relevant to in vivo conditions were described by different researchers. The aim of this study was to compare these methods and correlate them with in vivo results. Six series of ODTs were prepared by direct compression. Their mechanical properties and disintegration times were measured with pharmacopoeial and alternative methods and compared with the in vivo results. The highest correlation with oral disintegration time was f...
Orodispersible tablets disintegrate rapidly (within 3 minutes) in the oral cavity and release the m...
Formulation of a convenient dosage form for administration, by considering swallowing difficulty and...
Drug delivery systems are becoming increasingly sophisticated as pharmaceutical scientists acquire a...
AbstractEven that orodispersible tablets (ODTs) have been successfully used in therapy for more than...
Disintegration time is the key critical quality attribute for a tablet classed as an Orally Disinteg...
Disintegration time is the key critical quality attribute for a tablet classed as an Orally Disinteg...
The Author(s) 2013. This article is published with open access at Springerlink.com Background Orodis...
The purpose of this study was to evaluate the biopharmaceutical drug properties suitable for orally ...
MastersOrally Disintegrating Tablets (ODTs) have become a very popular dosage form as they disintegr...
The purpose of writing this review is Oral delivery is currently the gold standard in the pharmaceut...
An orally disintegrating tablet (ODT) is defined as a solid dosage form that dis-solves or disintegr...
Oral drug delivery remains the preferred route for administration of various drugs. Recent developme...
The availability of biorelevant methods for the disintegration study of pharmaceutical orodispersibl...
Objective. For rapidly disintegrating tablets (RDTs), the current USP method does not accurately mea...
Orodispersible dosage forms are intended to be placed on tongue where, in contact with limited saliv...
Orodispersible tablets disintegrate rapidly (within 3 minutes) in the oral cavity and release the m...
Formulation of a convenient dosage form for administration, by considering swallowing difficulty and...
Drug delivery systems are becoming increasingly sophisticated as pharmaceutical scientists acquire a...
AbstractEven that orodispersible tablets (ODTs) have been successfully used in therapy for more than...
Disintegration time is the key critical quality attribute for a tablet classed as an Orally Disinteg...
Disintegration time is the key critical quality attribute for a tablet classed as an Orally Disinteg...
The Author(s) 2013. This article is published with open access at Springerlink.com Background Orodis...
The purpose of this study was to evaluate the biopharmaceutical drug properties suitable for orally ...
MastersOrally Disintegrating Tablets (ODTs) have become a very popular dosage form as they disintegr...
The purpose of writing this review is Oral delivery is currently the gold standard in the pharmaceut...
An orally disintegrating tablet (ODT) is defined as a solid dosage form that dis-solves or disintegr...
Oral drug delivery remains the preferred route for administration of various drugs. Recent developme...
The availability of biorelevant methods for the disintegration study of pharmaceutical orodispersibl...
Objective. For rapidly disintegrating tablets (RDTs), the current USP method does not accurately mea...
Orodispersible dosage forms are intended to be placed on tongue where, in contact with limited saliv...
Orodispersible tablets disintegrate rapidly (within 3 minutes) in the oral cavity and release the m...
Formulation of a convenient dosage form for administration, by considering swallowing difficulty and...
Drug delivery systems are becoming increasingly sophisticated as pharmaceutical scientists acquire a...