The feasibility of injection molding was explored in the preparation of a novel capsular device for oral pulsatile/delayed delivery based on swellable/erodible polymers. For this purpose, a mold intended to be coupled with a bench-top injection-molding press was designed. This was expected to enable the preparation of matching capsule cap and body items within a single manufacturing cycle and the selection of differing shell thicknesses (300, 600, and 900 μm). Hydroxypropylcellulose (Klucel(®) EF, LF, and GF) was employed as the release-controlling polymer in admixture with polyethylene glycol 1500 (10%, w/w) as the plasticizer. After preliminary trials aimed at the setup of operating conditions, Klucel(®) EF and LF capsule shells with satisfactory technological properties were manufactured. The performance of capsular devices filled with a tracer drug powder was studied by means of a modified USP31 disintegration apparatus. Typical in vitro delayed release patterns were thereby obtained, with lag time increasing as a function of the wall thickness. A good correlation was found between the latter parameter and t (10%), i.e., the time to 10% release, for both polymer grades employed. On the basis of the overall results, the investigated technique was proven suitable for the manufacturing of an innovative pulsatile release platform.

A novel injection-molded capsular device for oral pulsatile delivery based on swellable/erodible polymers / A. Gazzaniga, M. Cerea, A. Cozzi, A. Foppoli, A. Maroni, L. Zema. - In: AAPS PHARMSCITECH. - ISSN 1530-9932. - 12:1(2011 Mar), pp. 295-303. [10.1208/s12249-011-9581-6]

A novel injection-molded capsular device for oral pulsatile delivery based on swellable/erodible polymers

A. Gazzaniga
Primo
;
M. Cerea
Secondo
;
A. Cozzi;A. Foppoli;A. Maroni
Penultimo
;
L. Zema
Ultimo
2011

Abstract

The feasibility of injection molding was explored in the preparation of a novel capsular device for oral pulsatile/delayed delivery based on swellable/erodible polymers. For this purpose, a mold intended to be coupled with a bench-top injection-molding press was designed. This was expected to enable the preparation of matching capsule cap and body items within a single manufacturing cycle and the selection of differing shell thicknesses (300, 600, and 900 μm). Hydroxypropylcellulose (Klucel(®) EF, LF, and GF) was employed as the release-controlling polymer in admixture with polyethylene glycol 1500 (10%, w/w) as the plasticizer. After preliminary trials aimed at the setup of operating conditions, Klucel(®) EF and LF capsule shells with satisfactory technological properties were manufactured. The performance of capsular devices filled with a tracer drug powder was studied by means of a modified USP31 disintegration apparatus. Typical in vitro delayed release patterns were thereby obtained, with lag time increasing as a function of the wall thickness. A good correlation was found between the latter parameter and t (10%), i.e., the time to 10% release, for both polymer grades employed. On the basis of the overall results, the investigated technique was proven suitable for the manufacturing of an innovative pulsatile release platform.
No
English
capsular device; hydroxypropylcellulose (HPC); injection molding; oral drug delivery; pulsatile/delayed release
Settore CHIM/09 - Farmaceutico Tecnologico Applicativo
Articolo
Esperti anonimi
Pubblicazione scientifica
mar-2011
Springer
12
1
295
303
9
Pubblicato
Periodico con rilevanza internazionale
NON aderisco
info:eu-repo/semantics/article
A novel injection-molded capsular device for oral pulsatile delivery based on swellable/erodible polymers / A. Gazzaniga, M. Cerea, A. Cozzi, A. Foppoli, A. Maroni, L. Zema. - In: AAPS PHARMSCITECH. - ISSN 1530-9932. - 12:1(2011 Mar), pp. 295-303. [10.1208/s12249-011-9581-6]
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Article (author)
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A. Gazzaniga, M. Cerea, A. Cozzi, A. Foppoli, A. Maroni, L. Zema
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/160836
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