Factors affecting drug release from hydroxypropyl methylcellulose matrix systems in the light of classical and percolation theories

被引:50
|
作者
Caraballo, Isidoro [1 ]
机构
[1] Univ Seville, Iberoameri Swiss Ctr Dev Dosage Forms CISDEM, Dept Pharm & Pharmaceut Technol, E-41012 Seville, Spain
关键词
controlled release; critical points; formulation factors; hydrophilic matrices; hydroxypropyl methylcellulose; percolation threshold; PARTICLE-SIZE; HYDROPHILIC MATRICES; CRITICAL-POINTS; HYDROXYPROPYLMETHYLCELLULOSE MATRICES; DELIVERY SYSTEM; SOLUTE RELEASE; TABLETS; HPMC; HYDROCHLORIDE; FORMULATION;
D O I
10.1517/17425247.2010.528199
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Areas covered in this review: A new approach, proposed in 2004, based on percolation theory to explain the influence of the main formulation factors on drug release from HPMC matrices has been analyzed, paying attention to the advantages with respect to previous theories. What the reader will gain: The influence of especially important factors such as polymer concentration and particle size is now much better known thanks to these new theories. Take home message: To formulate a HPMC matrix, the system must be above the polymer's critical point, that is, allowing HPMC to act as outer phase. In this way, a coherent gel layer will be obtained because the first moment and the drug release will be controlled by this layer. Furthermore, knowing the critical points allows the vicinity of these points to be avoided, which are regions of high variability. In this way, robust dosage forms can be obtained.
引用
收藏
页码:1291 / 1301
页数:11
相关论文
共 50 条
  • [21] Swelling of hydroxypropyl methylcellulose matrix tablets .2. Mechanistic study of the influence of formulation variables on matrix performance and drug release
    Gao, P
    Skoug, JW
    Nixon, PR
    Ju, TR
    Stemm, NL
    Sung, KC
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (07) : 732 - 740
  • [22] Controlled release of dual drug-loaded hydroxypropyl methylcellulose matrix tablet using drug-containing polymeric coatings
    Lee, BJ
    Ryu, SG
    Cui, JH
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 188 (01) : 71 - 80
  • [23] PREDICTION OF DRUG-RELEASE FROM HYDROXYPROPYL METHYLCELLULOSE (HPMC) MATRICES - EFFECT OF POLYMER CONCENTRATION
    SHAH, N
    ZHANG, GH
    APELIAN, V
    ZENG, FW
    INFELD, MH
    MALICK, AW
    PHARMACEUTICAL RESEARCH, 1993, 10 (11) : 1693 - 1695
  • [24] Factors affecting drug release from liposomes
    Lindner, Lars H.
    Hossann, Martin
    CURRENT OPINION IN DRUG DISCOVERY & DEVELOPMENT, 2010, 13 (01) : 111 - 123
  • [25] Influence of physico-chemical properties of hydroxypropyl methylcellulose on quetiapine fumarate release from sustained release matrix tablets
    Ellakwa, Takwa E.
    Abu-Khadra, Ahmad S.
    Ellakwa, Doha El-Sayed
    BMC CHEMISTRY, 2024, 18 (01)
  • [26] STUDYING THE IMPACT OF FORMULATION AND PROCESSING PARAMETERS ON THE RELEASE CHARACTERISTICS FROM HYDROXYPROPYL METHYLCELLULOSE MATRIX TABLETS OF DICLOFENAC
    Elzayat, Ehab M.
    Abdel-Rahman, Ali A.
    Ahmed, Sayed M.
    Alanazi, Fars K.
    Habib, Walid A.
    Sakr, Adel
    ACTA POLONIAE PHARMACEUTICA, 2016, 73 (02): : 439 - 452
  • [27] pH-Controlled drug release from mesoporous silica tablets coated with hydroxypropyl methylcellulose phthalate
    Xu, Wujun
    Gao, Qiang
    Xu, Yao
    Wu, Dong
    Sun, Yuhan
    MATERIALS RESEARCH BULLETIN, 2009, 44 (03) : 606 - 612
  • [28] Drug release optimization from microparticles of poly(ε-caprolactone) and hydroxypropyl methylcellulose polymeric blends: formulation and characterization
    Javed, I.
    Ranjha, N. M.
    Mahmood, K.
    Kashif, S.
    Rehman, M.
    Usman, F.
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2014, 24 (06) : 607 - 612
  • [29] Effect of hydrophilic excipient on drug release from ethylcellulose and hydroxypropyl methylcellulose films containing lidocain and prilocain
    Kouchak, M.
    Rezae, S.
    Moshabeh, N.
    TOXICOLOGY LETTERS, 2010, 196 : S251 - S251
  • [30] PERCOLATION EFFECTS IN MATRIX-TYPE CONTROLLED DRUG-RELEASE SYSTEMS
    LEUENBERGER, H
    BONNY, JD
    KOLB, M
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 115 (02) : 217 - 224