This study was supported in part by the Private University Research Branding Project from MEXT; a Grant-in-Aid for Scientific Research (C) (17K08249 [to T.K. and T.S.]) from the Japan Society for the Promotion of Science (JSPS); a grant for cooperative research from the Hamaguchi Foundation for the Advancement of Biochemistry [to T.S.], and the Takeda Science Foundation [to T.K.]. We thank Mr. Yuya Nito and Ms. Akiko Asami for their valuable technical assistance in conducting the experiments.

This animal study (#AP17P004) was performed in accordance with the guidelines approved by the Nihon University Animal Care and Use Committee (Tokyo, Japan). This study (#17-0001) was approved by the Radioisotope Center of the School of Pharmacy, Nihon University.
1. Animals Used for Intranasal Administration Under Inhalation Anesthesia
<ol>
	<li>House the experimental mice in stainless-steel cages under a 12-h light/dark cycle (light on 8:00 AM&#8211;8:00 PM), with a controlled temperature m...

<ol>
	<li>Sakane, T., Yamashita, S., Yata, N., Sezaki, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transnasal+delivery+of+5-fluorouracil+to+the+brain+in+the+rat.">Transnasal delivery of 5-fluorouracil to the brain in the rat.</a> Journal of Drug Targeting. 7 (3), 233-240 (1999).</li><li>Illum, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transport+of+drugs+from+the+nasal+cavity+to+the+central+nervous+system.">Transport of drugs from the nasal cavity to the central nervous system.</a> European Journal of Pharmaceutical Science. 11 (1), 1-18 (2000).</li><li>Hanson, L. R., Frey, W. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intranasal+delivery+bypasses+the+blood-brain+barrier+to+target+therapeutic+agents+to+the+central+nervous+system+and+treat+neurodegenerative+disease.">Intranasal delivery bypasses the blood-brain barrier to target therapeutic agents to the central nervous system and treat neurodegenerative disease.</a> BMC Neuroscience. 9 (Suppl 3), S5 (2008).</li><li>Chapman, C. D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intranasal+treatment+of+central+nervous+system+dysfunction+in+humans.">Intranasal treatment of central nervous system dysfunction in humans.</a> Pharmaceutical Research. 30 (10), 2475-2484 (2012).</li><li>Kanazawa, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Development+of+non-invasive+drug+delivery+system+to+the+brain+for+brain+diseases+therapy.">Development of non-invasive drug delivery system to the brain for brain diseases therapy.</a> Yakugaku-Zasshi. 138 (4), 443-450 (2018).</li><li>Kozlovskaya, L., Abou-Kaoud, M., Stepensky, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantitative+analysis+of+drug+delivery+to+the+brain+via+nasal+route.">Quantitative analysis of drug delivery to the brain via nasal route.</a> Journal of Controlled Release. 189, 133-140 (2014).</li><li>Hirai, S., Yashiki, T., Matsuzawa, T., Mima, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Absorption+of+drugs+from+the+nasal+mucosa+of+rat.">Absorption of drugs from the nasal mucosa of rat.</a> International Journal of Pharmaceutics. 7 (4), 317-325 (1981).</li><li>Lochhead, J. J., Thorne, R. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intranasal+delivery+of+biologics+to+the+central+nervous+system.">Intranasal delivery of biologics to the central nervous system.</a> Advances in Drug Delivery Reviews. 64 (7), 614-628 (2011).</li><li>Lalatsa, A., Schatzlein, A. G., Stepensky, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Strategies+to+deliver+peptide+drugs+to+the+brain.">Strategies to deliver peptide drugs to the brain.</a> Molecular Pharmaceutics. 11 (4), 1081-1093 (2014).</li><li>Kanazawa, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Brain+delivery+of+small+interfering+ribonucleic+acid+and+drugs+through+intranasal+administration+with+nano-sized+polymer+micelles.">Brain delivery of small interfering ribonucleic acid and drugs through intranasal administration with nano-sized polymer micelles.</a> Medical Devices. 8, 57-64 (2015).</li><li>Kanazawa, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enhancement+of+nose-to-brain+delivery+of+hydrophilic+macromolecules+with+stearate-+or+polyethylene+glycol-modified+arginine-rich+peptide.">Enhancement of nose-to-brain delivery of hydrophilic macromolecules with stearate- or polyethylene glycol-modified arginine-rich peptide.</a> International Journal of Pharmacology. 530 (1-2), 195-200 (2017).</li><li>Kamei, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effect+of+an+enhanced+nose-to-brain+delivery+of+insulin+on+mild+and+progressive+memory+loss+in+the+senescence-accelerated+mouse.">Effect of an enhanced nose-to-brain delivery of insulin on mild and progressive memory loss in the senescence-accelerated mouse.</a> Molecular Pharmaceutics. 14 (3), 916-927 (2017).</li><li>Suzuki, T., Oshimi, M., Tomono, K., Hanano, M., Watanabe, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Investigation+of+transport+mechanism+of+pentazocine+across+the+blood-brain+barrier+using+the+in+situ+rat+brain+perfusion+technique.">Investigation of transport mechanism of pentazocine across the blood-brain barrier using the in situ rat brain perfusion technique.</a> Journal of Pharmaceutical Science. 91 (11), 2346-2353 (2002).</li></ol>

The authors have nothing to disclose.

The nose-to-brain delivery of drugs is expected to have a pronounced effect on central nervous system disorders because this pathway represents a direct transportation route that bypasses the BBB. Three different nose-to-brain pathways have been reported to date8. The first is the olfactory nerve pathway, which passes from the olfactory mucosa in the nasal mucosa to the forebrain via the olfactory nerve. The second is the trigeminal nerve pathway, which passes from the respiratory mucosa in the na...

Biomedicines such as peptides, oligonucleotides, and antibodies are considered to have potential application as novel therapeutic agents for refractory central nervous system disorders that currently have no curative therapy. However, because most biomedicines are water-soluble macromolecules, delivery from the blood into the brain via intravenous or oral administration is extremely difficult due to impedance of the blood-brain barrier (BBB).
In recent years, intranasal administration has been reported to be a potential pathway for nose-to-brain delivery of therapeutic agents that avoids the BBB1,2,3,4,5. However, there have been relatively few reports regarding the quantitative analysis of nose-to-brain pathway delivery6. Moreover, there have been virtually no reports on established optimal administration conditions and dosing regimens, such as volume, times, time-periods, and speed, for investigations of nose-to-brain delivery. The aforementioned deficiencies can be ascribed to the following reasons: (i) an optimal method of intranasal administration for mice has yet to be established, and (ii) intranasal administration by pipetting, which is generally used, is typically characterized by interindividual variation among animals due to mucociliary clearance (MC), thereby often leading to underestimations of the actual nose-to-brain delivery potential of a particular drug.
Inhalation anesthesia using isoflurane (initiation: 4%, maintenance: 2%) with an inhalation mask for rodents has gained widespread use, with the aim of reducing or eliminating the pain associated with surgery performed on experimental animals. The use of masks makes it relatively straightforward to perform typical drug administration in experimental animals under inhalation anesthesia via the subcutaneous, intraperitoneal, and intravenous routes. However, in the case of intranasal administration, the mask needs to be temporarily removed from the animals for drug administration. With maintenance under 2% isoflurane, animals typically awaken rapidly from inhalation anesthesia. When the administration volume per dose is large, this could cause the drug solution to flow from the nasal cavity into the esophagus, and therefore a single large dose may need to be broken down into multiple smaller doses for intranasal administration to small animals. As intranasal administration necessitates mask removal for repeated administration and sufficient time for sustained nasal cavity delivery, there is a high probability that mice would awaken from anesthesia during the administration procedure. This makes it very difficult to perform intranasal administration under a stable anesthetic state, and probably contributes to the observed interindividual variation of nose-to-brain delivery among rodents.
In this study, we therefore developed two novel methods of stable intranasal administration under inhalation anesthesia, which impose minimal physical stress on the experimental animals. For the first method, we used a temporarily openable mask that enables intranasal administration during inhalation anesthesia. The openable part of the mask incorporates a silicone plug that can be used in accordance with administration timing to facilitate stable intranasal administration using a pipette. For the second method, a cannula was surgically inserted to pass from the esophagus into the nasal cavity, and a syringe pump was then attached to this so that the drug solution could be directly and reliably delivered into the nasal cavity under stable inhalation anesthesia. This method can enhance the delivery of drugs into the brain via the nose-to-brain route, because by substantially minimizing the effects of MC, drug retentively in the nasal cavity would be improved. In addition, we describe a method for quantitatively evaluating drug distribution levels (% for the injected dose/g brain) in the brain using radio-labeled [14C]-inulin [molecular weight (MW): 5,000] as a model substrate of water-soluble macromolecules.

<table>
	<tbody>
		<tr>
			<td>ddY mouse</td>
			<td>Japan SLC, Inc.</td>
			<td></td>
			<td>Male, 4-6 weeks, 20-30 g</td>
		</tr>
		<tr>
			<td>Isoflurane</td>
			<td>Pfizer</td>
			<td>v002139</td>
			<td></td>
		</tr>
		<tr>
			<td>Isoflurane setup</td>
			<td>SHINANO manufacturing CO. LTD.</td>
			<td>SN-487-OTAir, SN-489-4</td>
			<td></td>
		</tr>
		<tr>
			<td>Isoflurane mask</td>
			<td>SHINANO manufacturing CO. LTD.</td>
			<td></td>
			<td>For small rodents</td>
		</tr>
		<tr>
			<td>Isoflurane mask (Opneable type)</td>
			<td>SHINANO manufacturing CO. LTD.</td>
			<td></td>
			<td>Special orders</td>
		</tr>
		<tr>
			<td>Anesthesia Box</td>
			<td>SHINANO manufacturing CO. LTD.</td>
			<td>SN-487-85-02</td>
			<td></td>
		</tr>
		<tr>
			<td>Animal experiments scissors-1</td>
			<td>NATSUME SEISAKUSHO CO., LTD.</td>
			<td>B-27H</td>
			<td></td>
		</tr>
		<tr>
			<td>Animal experiments scissors-2</td>
			<td>NATSUME SEISAKUSHO CO., LTD.</td>
			<td>B-13H</td>
			<td></td>
		</tr>
		<tr>
			<td>Tweezers-1</td>
			<td>FINE SCIENCE TOOLS Inc.</td>
			<td>11272-30</td>
			<td>Dumont #7 Dumoxel</td>
		</tr>
		<tr>
			<td>Tweezers-2</td>
			<td>NATSUME SEISAKUSHO CO., LTD.</td>
			<td>A-12-1</td>
			<td></td>
		</tr>
		<tr>
			<td>Cannula tube (PE-50)</td>
			<td>Becton, Dickinson and Company.</td>
			<td>5069773</td>
			<td>I.D.: 0.58 mm, O.D.: 0.965 mm</td>
		</tr>
		<tr>
			<td>Cannula tube (SP-10)</td>
			<td>NATSUME SEISAKUSHO CO., LTD.</td>
			<td>KN-392</td>
			<td>I.D.: 0.28 mm, O.D.: 0.61 mm</td>
		</tr>
		<tr>
			<td>Shaver</td>
			<td>MARUKAN, LTD.</td>
			<td>DC-381</td>
			<td></td>
		</tr>
		<tr>
			<td>Stereoscopic microscope</td>
			<td>Olympus Corporation</td>
			<td>SZ61</td>
			<td></td>
		</tr>
		<tr>
			<td>Needle 27G 1/2 in 13 mm</td>
			<td>TERUMO CORPORATION</td>
			<td>NN-2738R</td>
			<td></td>
		</tr>
		<tr>
			<td>1 mL syringe</td>
			<td>TERUMO CORPORATION</td>
			<td>SS-01T</td>
			<td></td>
		</tr>
		<tr>
			<td>Syringe pump</td>
			<td>Neuro science</td>
			<td>NE-1000</td>
			<td></td>
		</tr>
		<tr>
			<td>Cellulose membrane</td>
			<td>Toyo Roshi Kaisya, Ltd.</td>
			<td>00011090</td>
			<td></td>
		</tr>
		<tr>
			<td>Micro spatula</td>
			<td>Shimizu Akira Inc.</td>
			<td>91-0088</td>
			<td></td>
		</tr>
		<tr>
			<td>Micropipette (0.5-10 uL)</td>
			<td>Eppendorf AG</td>
			<td>Z368083</td>
			<td></td>
		</tr>
		<tr>
			<td>Pipette chip</td>
			<td>Eppendorf AG</td>
			<td>0030 000.811</td>
			<td></td>
		</tr>
		<tr>
			<td>Tape</td>
			<td>TimeMed Labeling System, Inc.</td>
			<td>T-534-R</td>
			<td>For fixing mouse</td>
		</tr>
		<tr>
			<td>[14C]-Inulin</td>
			<td>American Radiolabeled Chemicals Inc.</td>
			<td>ARC0124A</td>
			<td>0.1 mCi/mL</td>
		</tr>
		<tr>
			<td>EtOH</td>
			<td>Wako Pure Chemical Industries, Ltd.</td>
			<td>054-00461</td>
			<td></td>
		</tr>
		<tr>
			<td>Liquid scintillation counter</td>
			<td>Perkin Elmer Life and Analytical Sciences, Inc</td>
			<td>Tri-Carb 4810TR</td>
			<td></td>
		</tr>
	</tbody>
</table>

novel methods for intranasal administration under inhalation anesthesia to evaluate nose-to-brain drug delivery

Intranasal administration has been reported to be a potential pathway for nose-to-brain delivery of therapeutic agents that circumvents the blood-brain barrier. However, there have been few reports regarding not only the quantitative analysis but also optimal administration conditions and dosing regimens for investigations of nose-to-brain delivery. The limited progress in research on nose-to-brain pathway mechanisms using rodents represents a significant impediment in terms of designing nose-to-brain delivery systems for candidate drugs.
To gain some headway in this regard, we developed and evaluated two novel methods of stable intranasal administration under inhalation anesthesia for experimental animals. We also describe a method for the evaluation of drug distribution levels in the brain via the nose-to-brain pathway using radio-labeled [14C]-inulin (molecular weight: 5,000) as a model substrate of water-soluble macromolecules.
Initially, we developed a pipette-based intranasal administration protocol using temporarily openable masks, which enabled us to perform reliable administration to animals under stable anesthesia. Using this system, [14C]-inulin could be delivered to the brain with little experimental error.
We subsequently developed an intranasal administration protocol entailing reverse cannulation from the airway side through the esophagus, which was developed to minimize the effects of mucociliary clearance (MC). This technique led to significantly higher levels of [14C]-inulin, which was quantitatively detected in the olfactory bulb, cerebrum, and medulla oblongata, than the pipette method. This appears to be because retention of the drug solution in the nasal cavity was substantially increased by active administration using a syringe pump in a direction opposite to the MC into the nasal cavity.
In conclusion, the two methods of intranasal administration developed in this study can be expected to be extremely useful techniques for evaluating pharmacokinetics in rodents. The reverse cannulation method, in particular, could be useful for evaluating the full potential of nose-to-brain delivery of drug candidates.

Figure 3 shows the [14C]-inulin levels (ID%&#8260;g brain) in the olfactory bulb (A), cerebrum (B), and medulla oblongata (C) obtained using the two types of intranasal administration assessed in the present study. Intranasal administration using the pipette method enabled delivery of [14C]-inulin into the brain using openable inhalation masks (Figure 1). Under inhalation anesthesia, the quantitative results...

Watch this Scientific Journal Video about Novel Methods for Intranasal Administration Under Inhalation Anesthesia to Evaluate Nose-to-Brain Drug Delivery at JoVE.com

Novel Methods for Intranasal Administration Under Inhalation Anesthesia to Evaluate Nose-to-Brain Drug Delivery

Here, we describe two novel methods of stable intranasal administration under inhalation anesthesia with minimal physical stress for experimental animals. We also describe a method for quantitative evaluation of drug distribution levels in the brain via the nose-to-brain pathway using radiolabeled [14C]-inulin as a model substrate of water-soluble macromolecules.

Intranasal administration has been reported to be a potential pathway for nose-to-brain delivery of therapeutic agents that circumvents the blood-brain ...

This method can help answer key questions in the pharmaceutical sciences field about intranasal administration and pharmacokinetics and pharmacology of drugs of interest. The main advantage of this technique is that it can be used for the quantitative evaluation of nose-to-brain delivery drug candidates and inhalation anesthesia with minimal stress to the animals. The implications of this technique extends towards the therapy of central nervous system diseases as it contributes to the development of drug delivery technologies via the nose-to-brain route.Demonstrating the procedure will be Mitsuyoshi Fukuda, a PhD student from my laboratory. For intranasal delivery via micropipette in an isolated radio isotope facility. Tape and anesthetize mouse to a cork board in the supine position, and administer 25 microliters of carbon-14 inulin solution in one to two microliter doses, alternatively, into the right and left nostrils of the animal.For reverse cannulation delivery from the airway side through the esophagus, place the anesthetized mouse under a dissecting microscope, and make a 1.5 centimeter skin incision over the throat. Use forceps to expand the incision until the trachea is exposed, and make a one millimeter incision in the exposed trachea. Insert a cannula 1.2 centimeters to the pre-marked position into the incision, and attach the opposite end of the cannula to the inside of an inhalation mask.After this, use forceps to expose the esophagus from under the trachea. Use scissors to make a one millimeter incision in the esophagus and insert a second cannula 1.4 centimeters to the pre-marked position toward the posterior end of the nasal cavity. It is important to insert cannula to an appropriate length according to the weight of the experimental animal and to adjust the length of the cannula in other ones.Ligate the esophageal cannula and attach a 27-gauge needle to a one milliliter syringe filled with an administration solution connected to a programmable microsyringe pump. Then deliver 25 microliters of carbon-14 inulin at a constant five microliter per minute rate until the entire volume of solution has been administered. A slow but constant diffusion rate is important for the retention of as much drug solution as possible within the nasal cavity.To quantify the amount of carbon-14 inulin that crossed the blood-brain barrier 30 minutes after the inulin administration, use scissors to carefully open the cranium of each experimentally-treated animal from the medulla oblongata side, and use a microspatula to carefully scoop out the brains. Place each brain on a piece of saline-moistened filter paper in a Petri dish on ice as it is harvested. And use a saline-soaked cotton swab to clean any blood from the surface of each brain.Next, quickly but carefully, dissect the brains into olfactory bulb, cerebrum, and medulla oblongata, plus pons sections. And place the brain samples in tissue solubilizer for one hour at 50 degrees Celsius, followed by the addition of 10 microliters of liquid scintillation cocktail. To determine the radioactivity of the applied solution, transfer a 25 microliter aliquot of the administration solution, dissolved in the scintillation cocktail, to a scintillation vial, and measure the disintegrations per minute of the carbon-14 radioactivity within the brain sample and the applied solution in a liquid scintillation counter.Under inhalation anesthesia, no experimental inter-individual variation is observed among intranasally-drug delivered animals. When the esophageal reverse cannula nasal cavity administration method is used, significantly higher levels of carbon-14 inulin are observed in the olfactory bulb, cerebrum, and medulla oblongata, than via micropipette delivery. Moreover, higher carbon-14 inulin is detected in the olfactory bulb and the medulla oblongata, both of which are prominently-evolved in the nose-to-brain pathway, than in the cerebrum.After its development, this technique paved the way for researchers in the field of nose-to-brain delivery to explore the bioactivity of large molecule therapeutic agents in the central nervous system.

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19.6K Görüntüleme.  Nihon University. Bu yöntem, farmasötik bilimler alanında intranazal yönetim, farmakokinetik ve ilgili ilaçların farmakolojisi ile ilgili anahtar soruların cevapverilmesine yardımcı olabilir. Bu tekniğin en büyük avantajı, burun-to-beyne doğum ilaç adaylarının kantitatif değerlendirilmesi ve hayvanlara en az stres ile inhalasyon anestezisi için kullanılabilir olmasıdır. Bu tekniğin etkileri, burundan beyne yol ile ilaç dağıtım teknolojilerinin gelişmesine katkıda olarak merkezi sin...