Insights into direct nose to brain delivery: current status and future perspective

被引:251
作者
Mittal, Deepti [1 ]
Ali, Asgar [1 ]
Md, Shadab [1 ]
Baboota, Sanjula [1 ]
Sahni, Jasjeet K. [1 ]
Ali, Javed [1 ]
机构
[1] Jamia Hamdard, Fac Pharm, Dept Pharmaceut, New Delhi, India
关键词
Blood-brain barrier; brain targeting; intranasal delivery; nanoparticles; olfactory pathway; INTRANASAL MUCOADHESIVE MICROEMULSIONS; FOCAL CEREBRAL-ISCHEMIA; CENTRAL-NERVOUS-SYSTEM; DRUG-DELIVERY; CHITOSAN NANOPARTICLES; TARGETING EFFICIENCY; LIPID NANOPARTICLES; MULTIPLE-SCLEROSIS; ALZHEIMERS-DISEASE; CLINICAL-EFFICACY;
D O I
10.3109/10717544.2013.838713
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Now a day's intranasal (i.n) drug delivery is emerging as a reliable method to bypass the blood-brain barrier (BBB) and deliver a wide range of therapeutic agents including both small and large molecules, growth factors, viral vectors and even stem cells to the brain and has shown therapeutic effects in both animals and humans. This route involves the olfactory or trigeminal nerve systems which initiate in the brain and terminate in the nasal cavity at the olfactory neuroepithelium or respiratory epithelium. They are the only externally exposed portions of the central nervous system (CNS) and therefore represent the most direct method of noninvasive entry into the brain. This approach has been primarily used to explore therapeutic avenues for neurological diseases. The potential for treatment possibilities with olfactory transfer of drugs will increase as more effective formulations and delivery devices are developed. Recently, the apomorphine hydrochloride dry powders have been developed for i.n. delivery (Apomorphine nasal, Lyonase technology, Britannia Pharmaceuticals, Surrey, UK). The results of clinical trial Phase III suggested that the prepared formulation had clinical effect equivalent to subcutaneously administered apomorphine. In coming years, intranasal delivery of drugs will demand more complex and automated delivery devices to ensure accurate and repeatable dosing. Thus, new efforts are needed to make this noninvasive route of delivery more efficient and popular, and it is also predicted that in future a range of intranasal products will be used in diagnosis as well as treatment of CNS diseases. This review will embark the existing evidence of nose-to-brain transport. It also provides insights into the most relevant pre-clinical studies of direct nose-brain delivery and delivery devices which will provide relative success of intranasal delivery system. We have, herein, outlined the relevant aspects of CNS drugs given intranasally to direct the brain in treating CNS disorders like Alzheimer's disease, depression, migraine, schizophrenia, etc.
引用
收藏
页码:75 / 86
页数:12
相关论文
共 71 条
[1]   Intranasal drug delivery of didanosine-loaded chitosan nanoparticles for brain targeting; an attractive route against infections caused by aids viruses [J].
Al-Ghananeem, Abeer M. ;
Saeed, Hayder ;
Florence, Rebecca ;
Yokel, Robert A. ;
Malkawi, Ahmad H. .
JOURNAL OF DRUG TARGETING, 2010, 18 (05) :381-388
[2]   Intranasal administration of nanostructured lipid carriers containing CNS acting drug: Pharmacodynamic studies and estimation in blood and brain [J].
Alam, M. Intakhab ;
Baboota, Sanjula ;
Ahuja, Alka ;
Ali, Mushir ;
Ali, Javed ;
Sahni, Jasjeet K. .
JOURNAL OF PSYCHIATRIC RESEARCH, 2012, 46 (09) :1133-1138
[3]  
Alam MI, 2011, CURR NANOSCI, V7, P1014
[4]   ENHANCED ORAL BIOAVAILABILITY OF DDI AFTER ADMINISTRATION OF 6-CL-DDP, AN ADENOSINE DEAMINASE-ACTIVATED PRODRUG, TO CHRONICALLY CATHETERIZED RATS [J].
ANDERSON, BD ;
MORGAN, ME ;
SINGHAL, D .
PHARMACEUTICAL RESEARCH, 1995, 12 (08) :1126-1133
[5]   REVISED ESTIMATE OF THE PREVALENCE OF MULTIPLE-SCLEROSIS IN THE UNITED-STATES [J].
ANDERSON, DW ;
ELLENBERG, JH ;
LEVENTHAL, CM ;
REINGOLD, SC ;
RODRIGUEZ, M ;
SILBERBERG, DH .
ANNALS OF NEUROLOGY, 1992, 31 (03) :333-336
[6]   FLUOXETINE FOR COCAINE DEPENDENCE IN METHADONE-MAINTENANCE [J].
BALON, R .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1994, 14 (05) :360-360
[7]   The triptan formulations: A critical evaluation [J].
Bigal, ME ;
Bordini, CA ;
Antoniazzi, AL ;
Speciali, JG .
ARQUIVOS DE NEURO-PSIQUIATRIA, 2003, 61 (2A) :313-320
[8]   Erythropoietin crosses the blood-brain barrier to protect against experimental brain injury [J].
Brines, ML ;
Ghezzi, P ;
Keenan, S ;
Agnello, D ;
de Lanerolle, NC ;
Cerami, C ;
Itri, LM ;
Cerami, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (19) :10526-10531
[9]   Comparative affinity of duloxetine and venlafaxine for serotonin and norepinephrine transporters in vitro and in vivo, human serotonin receptor subtypes, and other neuronal receptors [J].
Bymaster, FP ;
Dreshfield-Ahmad, LJ ;
Threlkeld, PG ;
Shaw, JL ;
Thompson, L ;
Nelson, DL ;
Hemrick-Luecke, SK ;
Wong, DT .
NEUROPSYCHOPHARMACOLOGY, 2001, 25 (06) :871-880
[10]   Future prospects of nanoparticles on brain targeted drug delivery [J].
Chakraborty, C. ;
Sarkar, B. ;
Hsu, C. H. ;
Wen, Z. H. ;
Lin, C. S. ;
Shieh, P. C. .
JOURNAL OF NEURO-ONCOLOGY, 2009, 93 (02) :285-286