Solid Dosage Forms of Biopharmaceuticals in Drug Delivery Systems Using Sustainable Strategies

被引:8
|
作者
Costa, Clarinda [1 ,2 ]
Casimiro, Teresa [1 ]
Corvo, Maria Luisa [2 ]
Aguiar-Ricardo, Ana [1 ]
机构
[1] Univ Nova Lisboa, NOVA Sch Sci & Technol, LAQV REQUIMTE, Dept Chem, P-2829516 Caparica, Portugal
[2] Univ Lisbon, Fac Farm, Inst Invest Medicamento iMed ULisboa, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
来源
MOLECULES | 2021年 / 26卷 / 24期
关键词
biopharmaceuticals; solid dosage forms; drying technologies; sustainable engineering; supercritical carbon dioxide; supercritical carbon dioxide-assisted spray-drying; FLUID-ASSISTED ATOMIZATION; DRY POWDER FORMULATIONS; SUPERCRITICAL CARBON-DIOXIDE; RAPID EXPANSION; MICROPARTICLES PRODUCTION; MICROMETRIC POWDERS; AQUEOUS-SOLUTIONS; SALICYLIC-ACID; THIN-FILMS; MICRONIZATION;
D O I
10.3390/molecules26247653
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drug delivery systems (DDS) often comprise biopharmaceuticals in aqueous form, making them susceptible to physical and chemical degradation, and therefore requiring low temperature storage in cold supply and distribution chains. Freeze-drying, spray-drying, and spray-freeze-drying are some of the techniques used to convert biopharmaceuticals-loaded DDS from aqueous to solid dosage forms. However, the risk exists that shear and heat stress during processing may provoke DDS damage and efficacy loss. Supercritical fluids (SCF), specifically, supercritical carbon dioxide (scCO(2)), is a sustainable alternative to common techniques. Due to its moderately critical and tunable properties and thermodynamic behavior, scCO(2) has aroused scientific and industrial interest. Therefore, this article reviews scCO(2)-based techniques used over the year in the production of solid biopharmaceutical dosage forms. Looking particularly at the use of scCO(2) in each of its potential roles-as a solvent, co-solvent, anti-solvent, or co-solute. It ends with a comparison between the compound's stability using supercritical CO2-assisted atomization/spray-drying and conventional drying.
引用
收藏
页数:19
相关论文
共 50 条
  • [31] Comprehensive review on additives of topical dosage forms for drug delivery
    Garg, Tarun
    Rath, Goutam
    Goyal, Amit K.
    DRUG DELIVERY, 2015, 22 (08) : 969 - 987
  • [32] Semi-Solid and Solid Dosage Forms for the Delivery of Phage Therapy to Epithelia
    Brown, Teagan L.
    Petrovski, Steve
    Chan, Hiu Tat
    Angove, Michael J.
    Tucci, Joseph
    PHARMACEUTICALS, 2018, 11 (01)
  • [33] Immediate drug release from solid oral dosage forms
    Schreiner, T
    Schaefer, UF
    Loth, H
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (01) : 120 - 133
  • [34] STABILIZATION OF A NEW ANTIULCER DRUG (LANSOPRAZOLE) IN THE SOLID DOSAGE FORMS
    TABATA, T
    MAKINO, T
    KASHIHARA, T
    HIRAI, S
    KITAMORI, N
    TOGUCHI, H
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1992, 18 (13) : 1437 - 1447
  • [35] An overview on dosage forms and formulation strategies for vaccines and antibodies oral delivery
    Madani, Faten
    Hsein, Hassana
    Busignies, Virginie
    Tchoreloff, Pierre
    PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2020, 25 (02) : 133 - 148
  • [36] SIGNIFICANCE OF DRUG CONTENT AND OF DRUG PROPORTION TO THE CONTENT UNIFORMITY OF SOLID DOSAGE FORMS
    EGERMANN, H
    PICHLER, E
    ACTA PHARMACEUTICA JUGOSLAVICA, 1988, 38 (04): : 279 - 286
  • [37] APPROACHES TO DEVELOPMENT OF SOLID - SELF MICRON EMULSIFYING DRUG DELIVERY SYSTEM: FORMULATION TECHNIQUES AND DOSAGE FORMS: A REVIEW
    Yetukuri, Koushik
    Sudheer, Preethi
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2012, 3 (10): : 3550 - 3558
  • [38] Impact of Excipient Interactions on Drug Bioavailability from Solid Dosage Forms
    Ravikiran Panakanti
    Ajit S. Narang
    Pharmaceutical Research, 2012, 29 : 2639 - 2659
  • [39] Impact of Excipient Interactions on Drug Bioavailability from Solid Dosage Forms
    Panakanti, Ravikiran
    Narang, Ajit S.
    PHARMACEUTICAL RESEARCH, 2012, 29 (10) : 2639 - 2659
  • [40] APPARATUS FOR DETERMINING RATE OF DRUG RELEASE FROM SOLID DOSAGE FORMS
    BAUN, DC
    WALKER, GC
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1969, 58 (05) : 611 - &