1996
DOI: 10.3109/03639049609069353
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Development and Characterization of a Buccoadhesive Dosage Form of Oxycodone Hydrochloride

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Cited by 86 publications
(39 citation statements)
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“…employed as a quality control procedure in pharmaceutical production and product development. Standard USP or BP dissolution apparatus have been used to study in vitro release profiles using both rotating elements, paddle [20,21,22] and basket. [23,24] Dissolution medium used for the study varied from 100-500 ml and speed of rotation from 50-100 rpm.…”
Section: -Drug Release Profilesmentioning
confidence: 99%
“…employed as a quality control procedure in pharmaceutical production and product development. Standard USP or BP dissolution apparatus have been used to study in vitro release profiles using both rotating elements, paddle [20,21,22] and basket. [23,24] Dissolution medium used for the study varied from 100-500 ml and speed of rotation from 50-100 rpm.…”
Section: -Drug Release Profilesmentioning
confidence: 99%
“…In vitro drug release studies have been employed as a quality control procedure in pharmaceutical production and product development. Standard USP or BP dissolution apparatus have been used to study in vitro release profiles using both rotating elements, paddle [17][18][19][20] and basket [21,22]. Dissolution medium used for the study varied from 100-500ml and speed of rotation from 50-100rpm.…”
Section: Drug Release Profiles [16]mentioning
confidence: 99%
“…A modified balance method (Parodi et al, 1996) was used to determine the bioadhesive performance of the ocular minitablets by measuring the force required to detach the tablets from a mucosal surface. The instrument is broadly composed of a modified two arm physical balance in which the right pan had been replaced by a glass plate (4 × 4 cm).…”
Section: Bioadhesion Potential Of Insertsmentioning
confidence: 99%