The effects of the treatment conditions on the dissolution profile of ethylcellulose coated pellets

被引:4
|
作者
Pavlokova, Sylvie [1 ]
Muselik, Jan [1 ]
Sabadkova, Dana [1 ]
Bernatova, Silvie [2 ]
Samek, Ota [2 ]
Neumann, David [3 ]
Franc, Ales [1 ]
机构
[1] Univ Vet & Pharmaceut Sci, Dept Pharmaceut, Palackeho Tr 1946-1, Brno 61242, Czech Republic
[2] Czech Acad Sci, ISI, Vvi, Kralovopolska 147, Brno 61264, Czech Republic
[3] Charles Univ Prague, Fac Med Hradec Kralove, Dept Pediat, Univ Hosp Hradec Kralove, Hradec Kralove, Czech Republic
关键词
Coated pellets; Wet treatment; Coating penetration; Pellet volume increase; Stability; DRUG-RELEASE; MORPHOLOGICAL PROPERTIES; MECHANICAL-PROPERTIES; POLYMER DISPERSIONS; GLUCOSE; CELLULOSE; HYPOGLYCEMIA; FORMULATION; PREVENTION; PLASTICIZERS;
D O I
10.1016/j.ejps.2019.02.034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Due to the additional particle coalescence in the coating, changes in the dissolution profile occur over time in the formulations coated by aqueous ethylcellulose latex. Dry thermal treatment (DT) of the coating can be used as a prevention of this process. Alternatively, it is advisable to take advantage of the synergistic effect of high humidity during wet treatment (WT), which substantially accelerates the film formation. This can be a problem for time-controlled systems, which are based on the coating rupture due to the penetration of water into the core causing the increase in the system volume. This process can begin already during the WT, which may affect the coating adversely. The submitted work was focused on the stability testing of two pellet core compositions: pellets containing swelling superdisintegrant sodium carboxymethyl starch (CMS) and pellets containing osmotically active polyethylene glycol (PEG). Another objective was to identify the treatment/storage condition effects on the pellet dissolution profiles. These pellets are intended to prevent hypoglycemia for patients with diabetes mellitus and therefore, besides the excipients, pellet cores contain 75% or 80% of glucose. The pellet coating is formed by ethylcellulose-based latex, which provides the required lag time (120-360 min). The sample stability was evaluated depending on the pellet core composition (PEG, CMS) for two types of final pellet coating treatment (DT or WT). Scanning electron microscopy and Raman microspectroscopy revealed the penetration of glucose and polyethylene glycol from the core to the PEG pellet surface after WT. For the CMS sample, significant pellet swelling after WT (under the conditions of elevated humidity) was statistically confirmed by the means of stereomicroscopic data evaluation. Therefore, the acceleration of dissolution rate during the stress tests is caused by the soluble substance penetration through the coating in the case of PEG pellets or by dosage form volume increase in the case of CMS pellets. The observed mechanisms can be generally anticipated during the stability testing of the ethylcellulose coated dosage forms. The aforementioned processes do not occur after DT and the pellets are stable in the environment without increased humidity.
引用
收藏
页码:86 / 95
页数:10
相关论文
共 50 条
  • [1] Effects of pharmaceutical processes on the quality of ethylcellulose coated pellets: Quality by design approach
    Thapa, Prakash
    Thapa, Ritu
    Choi, Du Hyung
    Jeong, Seong Hoon
    POWDER TECHNOLOGY, 2018, 339 : 25 - 38
  • [2] PROBABILISTIC MODELS FOR DISSOLUTION OF ETHYLCELLULOSE COATED MICROSPHERES
    Bezbradica, Marija
    Barat, Ana
    Ruskin, Heather J.
    Crane, Martin
    EUROPEAN SIMULATION AND MODELLING CONFERENCE 2010, 2010, : 408 - 412
  • [3] Prediction of drug release from ethylcellulose coated pellets
    Muschert, S.
    Siepmann, F.
    Leclercq, B.
    Carlin, B.
    Siepmann, J.
    JOURNAL OF CONTROLLED RELEASE, 2009, 135 (01) : 71 - 79
  • [4] Influence of the type of enteric coating suspension, coating layer and process conditions on dissolution profile and stability of coated pellets of diclofenac sodium
    Albanez, Roberta
    Nitz, Marcello
    Taranto, Osvaldir Pereira
    POWDER TECHNOLOGY, 2015, 269 : 185 - 192
  • [5] MECHANISM OF RELEASE FROM PELLETS COATED WITH AN ETHYLCELLULOSE-BASED FILM
    OZTURK, AG
    OZTURK, SS
    PALSSON, BO
    WHEATLEY, TA
    DRESSMAN, JB
    JOURNAL OF CONTROLLED RELEASE, 1990, 14 (03) : 203 - 213
  • [6] EFFECT OF SUBSTRATE ON MASS RELEASE FROM ETHYLCELLULOSE LATEX COATED PELLETS
    NESBITT, RU
    MAHJOUR, M
    MILLS, NL
    FAWZI, MB
    JOURNAL OF CONTROLLED RELEASE, 1994, 32 (01) : 71 - 77
  • [7] Adjustment of drug release kinetics from ethylcellulose-coated pellets
    Siepmann, F.
    Wahle, C.
    Zach, S.
    Leclercq, B.
    Carlin, B.
    Siepmann, J.
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2006, 58 : A50 - A50
  • [8] Evaluation of ethylcellulose-coated pellets optimized using the approach of Taguchi
    Palmieri, GF
    Wehrle, P
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1997, 23 (11) : 1069 - 1077
  • [9] Dissolution profile and solvent-uptake stability of theophylline containing pellets coated by methacrylate copolymers
    Lengyel, M
    Dávid, AZ
    Dredán, J
    Klebovich, I
    Antal, I
    EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 25 : S150 - S151
  • [10] Improved storage stability of controlled release pellets coated with aqueous ethylcellulose dispersion
    Muschert, S.
    Siepmann, F.
    Leclercq, B.
    Carlin, B.
    Siepmann, J.
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2007, 59 : A58 - A58