Bioavailability Enhancement Strategies: Basics, Formulation Approaches and Regulatory Considerations

被引:58
作者
Beg, Sarwar [1 ]
Swain, Suryakanta [2 ]
Rizwan, Md. [3 ]
Irfanuddin, Md. [4 ]
Malini, D. Shobha [5 ]
机构
[1] Jamia Hamdard, Fac Pharm, Dept Pharmaceut, New Delhi 110062, India
[2] Roland Inst Pharmaceut Sci, Dept Pharmaceut, Berhampur 760010, Orissa, India
[3] Wockhardt Res Ctr, Aurangabad, Maharashtra, India
[4] London Sch Commerce, London SW1 1NX, England
[5] MKCG Med Coll, Dept Community Med, Berhampur 760010, Orissa, India
关键词
Bioavailability; lipids; permeability; solubility; regulatory considerations; SOLID LIPID NANOPARTICLES; DRUG-METABOLISM BARRIERS; IMPROVED ORAL DELIVERY; IN-VITRO DIGESTION; LYMPHATIC TRANSPORT; ACTIVE SECRETION; EPITHELIAL-CELLS; POOR SOLUBILITY; SOLUBLE DRUGS; ABSORPTION;
D O I
10.2174/156720111797635504
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Poor solubility remains a major challenge for pharmaceutical industry, which is now considered to be an area of prime importance in the field of biomedical research. Approximately 40% new molecular entities (NMEs) synthesized in pharmaceutical R&Ds with advanced combinatorial chemistry and computer aided drug designing (CADD) approaches suffer from poor solubility and bioavailability related issues. Apart from these presence of intestinal tight junctional epithelial cells, transporters and enzymatic barriers further reduces the oral absorption of drugs. Implication of the novel lipid based nanocarriers and nanomaterials like dendrimers and carbon nanotubes as a delivery system can effectively enhance the oral bioavailability of drugs by breaching the barriers, and resolve all critics related to solubility and bioavailability. Thus prime objectives of this review are to give in-depth knowledge and critical appraisal on the barriers for poor oral bioavailability of drugs, along with various novel formulation approaches used for bioavailability enhancement such as lipid based formulations, nanosizing techniques, complexation with polymers and nanomaterials like dendrimers, carbon nanotubes, and penetration enhancers. Also it gives a brief account on in vitro, in vivo screening methods used for assessment of oral bioavailability, and regulatory considerations for the approval.
引用
收藏
页码:691 / 702
页数:12
相关论文
共 100 条
[1]
A new self-emulsifying drug delivery system (SEDDS) for poorly soluble drugs: Characterization, dissolution, in vitro digestion and incorporation into solid pellets [J].
Abdalla, Ahmed ;
Klein, Sandra ;
Maedder, Karsten .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 35 (05) :457-464
[2]
Acusphere's Hydrophobic Drug Delivery Systems (HDDSTM), ACUSPHERES HYDROPHOB
[3]
Predicting the impact of physiological and biochemical processes on oral drug bioavailability [J].
Agoram, B ;
Woltosz, WS ;
Bolger, MB .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 50 :S41-S67
[4]
Physicochemical properties of antifungal drug-cyclodextrin complexes prepared by supercritical carbon dioxide and by conventional techniques [J].
Al-Marzouqi, Ali H. ;
Elwy, Hanan M. ;
Shehadi, Ihsan ;
Adem, Abdu .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2009, 49 (02) :227-233
[5]
Formulation and biological evaluation of glimepiride-cyclodextrin-polymer systems [J].
Ammar, HO ;
Salama, HA ;
Ghorab, M ;
Mahmoud, AA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 309 (1-2) :129-138
[6]
Interspecies diversity of the occludin sequence: cDNA cloning of human, mouse, dog, and rat-kangaroo homologues [J].
AndoAkatsuka, Y ;
Saitou, M ;
Hirase, T ;
Kishi, M ;
Sakakibara, A ;
Itoh, M ;
Yonemura, S ;
Furuse, M ;
Tsukita, S .
JOURNAL OF CELL BIOLOGY, 1996, 133 (01) :43-47
[7]
[Anonymous], SOLVO IN VITRO TRANS
[8]
[Anonymous], SOL POORL WAT SOL DR
[9]
[Anonymous], SOLUBILITY BIOAVAILA
[10]
[Anonymous], M CHALLENGES POORLY