Evidence map›Paper›PMID 40501602›Full record

ArticlebioRxiv : the preprint server for biology2025

In-dwelling microfluidic device for precise and reliable intranasal drug delivery during freely-moving behavior.

Maria F Ramirez, Abhishek Gour, Sarah E Sniffen, Emma K Watson, Abhisheak Sharma, Daniel W Wesson

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Maria F RamirezDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Florida Chemical Senses Institute, Center for Addiction Research and Education, FL 32610, USA.
Abhishek GourDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, FL 32610, USA.
Sarah E SniffenDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Florida Chemical Senses Institute, Center for Addiction Research and Education, FL 32610, USA.
Emma K WatsonDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Florida Chemical Senses Institute, Center for Addiction Research and Education, FL 32610, USA.
Abhisheak SharmaDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, FL 32610, USA.
Daniel W WessonDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Florida Chemical Senses Institute, Center for Addiction Research and Education, FL 32610, USA.

Funding

Circuitry and function of ventral striatum subregionsR01DA049449 · NIDA · UNIVERSITY OF FLORIDA · PI MA, MINGHONG, WESSON, DANIEL W · 2020 to 2024
$2.1M
NIDA NIH HHS R01 DA049449
6 · The paper itself

Abstract

Many substances/drugs are administered intranasally (IN). These include opioid overdose reversal drugs, anti-epileptic medications, migraine medications, hormone treatments, and medicines to treat/prevent allergies, colds, and flues including nasally-administered vaccines, corticosteroids, antihistamines, and decongestants. Additionally, IN administration is the preferred route of entry by users of illicit drugs. Despite the widespread use of the IN route of administration, there is no established paradigm to access this route of administration preclinically to yield precise and reliable control over delivery. This poses major gaps in therapeutic discovery/testing, establishing pharmacokinetic/pharmacodynamic relationships of therapeutics, and understanding the mechanisms of actions of therapeutics. We developed an in-dwelling microfluidic device, that, when implanted upon the nasal bone, accesses the nasal cavity to allow reliable and precise IN fluid delivery during freely-moving behavior. We validated this device, called the Nasal Access Port (NAP), to confirm it allows rapid and precise control of fluids. We further exemplified the application of the NAP for studying outcomes of IN cocaine in mice, including its pharmacokinetic profile, and both the rapid release of dopamine (DA) and behavioral effects upon IN cocaine. By achieving precise and reliable access to the IN route of administration, the NAP represents a significant methodological advance with broad applicability in the biomedical and life sciences, especially in the neuroscience, pharmacology, medicinal chemistry, and physiology domains.

Identifiers

PMID40501602
PMCPMC12154640

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.