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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Annals of Clinical and Experimental Neurology</journal-id><journal-title-group><journal-title xml:lang="en">Annals of Clinical and Experimental Neurology</journal-title><trans-title-group xml:lang="ru"><trans-title>Анналы клинической и экспериментальной неврологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-5473</issn><issn publication-format="electronic">2409-2533</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1450</article-id><article-id pub-id-type="doi">10.17816/ACEN.1450</article-id><article-id pub-id-type="edn">QROQMW</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Comparative analysis of methods used for assessing blood-brain barrier permeability with fluorescent probes in laboratory animals</article-title><trans-title-group xml:lang="ru"><trans-title>Сравнительный анализ методов оценки проницаемости гематоэнцефалического барьера с использованием флуоресцентных зондов у экспериментальных животных</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0007-4195-2533</contrib-id><name-alternatives><name xml:lang="en"><surname>Berdnikov</surname><given-names>Arseniy K.</given-names></name><name xml:lang="ru"><surname>Бердников</surname><given-names>Арсений Константинович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>postgraduate student, Laboratory of neurobiology and tissue engineering, Brain Institute</p></bio><bio xml:lang="ru"><p>аспирант лаб. нейробиологии и тканевой инженерии Института мозга</p></bio><email>annaly-nevrologii@neurology.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1284-6711</contrib-id><name-alternatives><name xml:lang="en"><surname>Averchuk</surname><given-names>Anton S.</given-names></name><name xml:lang="ru"><surname>Аверчук</surname><given-names>Антон Сергеевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Biol.), Assoc. Prof., senior researcher, Laboratory of neurobiology and tissue engineering, Brain Institute</p></bio><bio xml:lang="ru"><p>канд. биол. наук, доцент, с. н. с. лаб. нейробиологии и тканевой инженерии Института мозга</p></bio><email>annaly-nevrologii@neurology.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5742-8356</contrib-id><name-alternatives><name xml:lang="en"><surname>Komleva</surname><given-names>Yulia K.</given-names></name><name xml:lang="ru"><surname>Комлева</surname><given-names>Юлия Константиновна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Dr. Sci. (Med.), leading researcher, Laboratory of neurobiology and tissue engineering, Brain Institute</p></bio><bio xml:lang="ru"><p>д-р мед. наук, в. н. с. лаб. нейробиологии и тканевой инженерии Института мозга</p></bio><email>annaly-nevrologii@neurology.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9743-8700</contrib-id><name-alternatives><name xml:lang="en"><surname>Potapenko</surname><given-names>Ilia V.</given-names></name><name xml:lang="ru"><surname>Потапенко</surname><given-names>Илья Викторович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, researcher, Laboratory of neurobiology and tissue engineering, Brain Institute</p></bio><bio xml:lang="ru"><p>PhD, н. с. лаб. нейробиологии и тканевой инженерии Института мозга</p></bio><email>annaly-nevrologii@neurology.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4012-6348</contrib-id><name-alternatives><name xml:lang="en"><surname>Salmina</surname><given-names>Alla B.</given-names></name><name xml:lang="ru"><surname>Салмина</surname><given-names>Алла Борисовна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Dr. Sci. (Med.), Professor, Corr. Member of the RAS, principal researcher, Head, Laboratory of neurobiology and tissue engineering, Deputy director, Brain Institute</p></bio><bio xml:lang="ru"><p>д-р мед. наук, профессор, член-корр. РАН, заместитель директора, г. н. с., зав. лаб. нейробиологии и тканевой инженерии Института мозга</p></bio><email>annaly-nevrologii@neurology.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Russian Center of Neurology and Neurosciences</institution></aff><aff><institution xml:lang="ru">Российский центр неврологии и нейронаук</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2026-04-07" publication-format="electronic"><day>07</day><month>04</month><year>2026</year></pub-date><volume>20</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>67</fpage><lpage>75</lpage><history><date date-type="received" iso-8601-date="2025-11-17"><day>17</day><month>11</month><year>2025</year></date><date date-type="accepted" iso-8601-date="2025-12-01"><day>01</day><month>12</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2026, Berdnikov A.K., Averchuk A.S., Komleva Y.K., Potapenko I.V., Salmina A.B.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2026, Бердников А.К., Аверчук А.С., Комлева Ю.К., Потапенко И.В., Салмина А.Б.</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="en">Berdnikov A.K., Averchuk A.S., Komleva Y.K., Potapenko I.V., Salmina A.B.</copyright-holder><copyright-holder xml:lang="ru">Бердников А.К., Аверчук А.С., Комлева Ю.К., Потапенко И.В., Салмина А.Б.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://annaly-nevrologii.com/pathID/article/view/1450">https://annaly-nevrologii.com/pathID/article/view/1450</self-uri><abstract xml:lang="en"><p><bold>Introduction.</bold> The blood-brain barrier (BBB) is a component of the neurovascular unit and a system regulating chemical homeostasis in brain tissue. Assessment of BBB permeability under normal and abnormal states of the central nervous system is of significant interest for experimental research in neuroscience. In recent years, there has been a substantial expansion of protocols that can be used to address such research tasks. Understanding the key differences, advantages, and limitations of each BBB investigation method is crucial for proper experimental design and data interpretation.</p> <p><bold>The aim</bold> of this review is to analyze modern methods for assessing BBB permeability in laboratory animals using fluorescent probes (tracers), provide their comparative characteristics, and evaluate selection criteria for solving experimental tasks.</p> <p><bold>Conclusion. </bold>Fluorescent probes enable real-time monitoring of BBB status in vivo during experimental neuroscience studies when assessing structural and functional integrity of the barrier in neuroinflammation, neurodegeneration, and brain tissue injury. Proper selection of fluorescent probes allows differentiated evaluation of para- and transcellular BBB permeability, vascular wall structure, and processes associated with brain tissue clearance.</p></abstract><trans-abstract xml:lang="ru"><p><bold>Введение.</bold> Гематоэнцефалический барьер (ГЭБ) является компонентом нейроваскулярной единицы и системой, регулирующей химический гомеостаз в ткани головного мозга. Оценка проницаемости ГЭБ в норме и при патологических состояниях центральной нервной системы представляет значительный интерес при проведении экспериментальных исследований в области нейронаук. В последние годы существенно расширился спектр протоколов, которые могут быть использованы для решения таких исследовательских задач. Понимание ключевых различий, достоинств и ограничений каждого метода исследования ГЭБ важно для корректного проведения экспериментов и интерпретации полученных данных.</p> <p><bold>Цель</bold> обзора — анализ современных методов оценки проницаемости ГЭБ у экспериментальных животных с использованием флуоресцентных зондов (трейсеров), их сравнительная характеристика и оценка критериев выбора для решения экспериментальных задач.</p> <p><bold>Заключение. </bold>Использование флуоресцентных зондов предоставляет возможность регистрировать состояние ГЭБ in vivo в экспериментальных нейронауках при оценке структурно-функциональной целостности барьера при нейровоспалении, нейродегенерации, повреждении ткани головного мозга. Правильный выбор флуоресцентного зонда позволяет дифференцированно оценить состояние пара- и трансцеллюлярной проницаемости ГЭБ, структуру сосудистой стенки и процессы, связанные с клиренсом ткани головного мозга.</p></trans-abstract><kwd-group xml:lang="en"><kwd>blood-brain barrier</kwd><kwd>permeability</kwd><kwd>fluorescent tracers</kwd><kwd>visualization</kwd><kwd>neurodegeneration</kwd><kwd>neuroinflammation</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>гематоэнцефалический барьер</kwd><kwd>проницаемость</kwd><kwd>флуоресцентные трейсеры</kwd><kwd>визуализация</kwd><kwd>нейродегенерация</kwd><kwd>нейровоспаление</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="en">Russian Science Foundation</institution></institution-wrap><institution-wrap><institution xml:lang="ru">Российский научный фонд</institution></institution-wrap></funding-source><award-id>22-15-00126-П</award-id></award-group><funding-statement xml:lang="en">The study was conducted with support from RSF grant No. 22-15-00126-П, https://rscf.ru/en/project/22-15-00126/</funding-statement><funding-statement xml:lang="ru">Исследование проведено при поддержке гранта РНФ № 22-15-00126-П, https://rscf.ru/en/project/22-15-00126/</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Salmina AB, Kharitonova EV, Gorina YV, et al. Blood–brain barrier and neurovascular unit in vitro models for studying mitochondria-driven molecular mechanisms of neurodegeneration. Int J Mol Sci. 2021;22(9):4661. doi: 10.3390/ijms22094661</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Siegenthaler JA, Sohet F, Daneman R. Sealing off the CNS: cellular and molecular regulation of blood-brain barriergenesis. Curr Opin Neurobiol. 2013;23(6):1057–1064. doi: 10.1016/j.conb.2013.06.006</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Schofield CL, Rodrigo-Navarro A, Dalby MJ, et al. Biochemical- and biophysical-induced barriergenesis in the blood–brain barrier: a review of barriergenic factors for use in in vitro models. Adv NanoBiomed Res. 2021;1(5):2000068. doi: 10.1002/anbr.202000068</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Аверчук А.С., Кукла М.В., Розанова Н.А. и др. Сравнительный анализ нейрогенеза и церебрального ангиогенеза в нейрогенной нише гиппокампа у животных с двумя моделями экспериментальной болезни Альцгеймера. Анналы клинической и экспериментальной неврологии. 2025;19(2):41–51. / Averchuk AS, Kukla MV, Rozanova NA, et al. Comparative analysis of neurogenesis and cerebral angiogenesis in the hippocampal neurogenic niche in animals with two experimental models of Alzheimer’s disease. Annals of Clinical and Experimental Neurology. 2025;19(2):41–51. doi: 10.17816/ACEN.1227</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Chaves JCS, Dando SJ, White AR, et al. Blood-brain barrier transporters: an overview of function, dysfunction in Alzheimer’s disease and strategies for treatment. Biochim Biophys Acta Mol Basis Dis. 2024;1870(2):166967. doi: 10.1016/j.bbadis.2023.166967</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Zhao Z, Nelson AR, Betsholtz C, et al. Establishment and dysfunction of the blood–brain barrier. Cell. 2015;163(5):1064–1078. doi: 10.1016/j.cell.2015.10.067</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Hirohashi T, Terasaki T, Shigetoshi M, et al. In vivo and in vitro evidence for nonrestricted transport of 2′,7′-Bis(2-Carboxyethyl)-5(6)-Carboxyfluorescein Tetraacetoxymethyl Ester at the blood–brain barrier. J Pharmacol Exp Ther. 1997;280(2):813–819.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Салмина А.Б. Метаболическая пластичность развивающегося и стареющего головного мозга. Нейрохимия. 2023;40(3):197–210. / Salmina AB. Metabolic plasticity of a developing and aging brain. Neurochemical Journal. 2023;40(3):197–210. doi: 10.31857/S1027813323030159</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Shao Y, Mai L, Qiao R, et al. Endothelial mitochondria in the blood-brain barrier. Fluids Barriers CNS. 2025;22(1):88. doi: 10.1186/s12987-025-00699-w</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Ghosh C, Hossain M, Solanki J, et al. Pathophysiological implications of neurovascular P450 in brain disorders. Drug Discovery Today. 2016;21(10):1609–1619. doi: 10.1016/j.drudis.2016.06.004</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Wang Y, Wu J, Wang J, et al. Mitochondrial oxidative stress in brain microvascular endothelial cells: triggering blood–brain barrier disruption. Mitochondrion. 2023;69:71–82. doi: 10.1016/j.mito.2023.01.007</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Sun J, Li H, Wang J, et al. Application of biomimetic approaches in the treatment of neurological disorders. Materials Today Bio. 2025;35:102334. doi: 10.1016/j.mtbio.2025.102334</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Salmina AB, Komleva YK, Lopatina OL, et al. Pericytes in Alzheimer’s disease: novel clues to cerebral amyloid angiopathy pathogenesis. Adv Exp Med Biol. 2019;1147:147–166. doi: 10.1007/978-3-030-16908-4_7</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Горина Я.В., Осипова Е.Д., Моргун А.В. и др. Аберрантный ангиогенез в ткани головного мозга при экспериментальной болезни Альцгеймера. Бюллетень сибирской медицины. 2020;19(4):46–52. / Gorina YaV, Osipova ED, Morgun AV, et al. Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease. Bulletin of Siberian Medicine. 2020;19(4):46–52. doi: 10.20538/1682-0363-2020-4-46-52</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Nguyen B, Bix G, Yao Y. Basal lamina changes in neurodegenerative disorders. Mol Neurodegeneration. 2021;16(1):81. doi: 10.1186/s13024-021-00502-y</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Alkhalifa AE, Al-Ghraiybah NF, Odum J, et al. Blood–brain barrier breakdown in Alzheimer’s disease: mechanisms and targeted strategies. Int J Mol Sci. 2023;24(22):16288. doi: 10.3390/ijms242216288</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Nehra G, Bauer B, Hartz AMS. Blood–brain barrier leakage in Alzheimer’s disease: from discovery to clinical relevance. Pharmacol Ther. 2022;234:108119. doi: 10.1016/j.pharmthera.2022.108119</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Lowenstein P. Crossing the Rubicon. Nat Biotechnol. 2009;27(1):42–44. doi: 10.1038/nbt0109-42</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Swissa E, Monsonego U, Yang LT, et al. Cortical plasticity is associated with blood–brain barrier modulation. Elife. 2024;12:RP89611. doi: 10.7554/eLife.89611</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Li Y, Li M, Zuo L, et al. Compromised blood–brain barrier integrity is associated with total magnetic resonance imaging burden of cerebral small vessel disease. Front Neurol. 2018;9:221. doi: 10.3389/fneur.2018.00221</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Goldim MPS, Della Giustina A, Petronilho F. Using evans blue dye to determine blood–brain barrier integrity in rodents. Curr Protoc Immunol. 2019;126(1):e83. doi: 10.1002/cpim.83</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Ryu HW, Lim W, Jo D, et al. Low-dose evans blue dye for near-infrared fluorescence imaging in photothrombotic stroke model. Int J Med Sci. 2018;15(7):696–702. doi: 10.7150/ijms.24257</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Saunders NR, Dziegielewska KM, Møllgård K, et al. Markers for blood–brain barrier integrity: how appropriate is Evans blue in the twenty-first century and what are the alternatives? Front Neurosci. 2015;9:385. doi: 10.3389/fnins.2015.00385</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Wu Q, Wei C, Guo S, et al. Acute iron overload aggravates blood–brain barrier disruption and hemorrhagic transformation after transient focal ischemia in rats with hyperglycemia. IBRO Neurosci Rep. 2022;13:87–95. doi: 10.1016/j.ibneur.2022.06.006</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Dash PK, Zhao J, Kobori N, et al. Activation of Alpha 7 cholinergic nicotinic receptors reduce blood–brain barrier permeability following experimental traumatic brain injury. J Neurosci. 2016;36(9):2809–2818. doi: 10.1523/JNEUROSCI.3197-15.2016</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Sindi M, Klees D, Dobelmann V, et al. Flecainide mediated sodium channel blockade enhances blood brain barrier integrity and promotes neuroprotection in neuroinflammation. Sci Rep. 2025;15(1):31032. doi: 10.1038/s41598-025-15430-w</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Ye LY, Sun LX, Zhong XH, et al. The structure of blood–tumor barrier and distribution of chemotherapeutic drugs in non-small cell lung cancer brain metastases. Cancer Cell Int. 2021;21(1):556. doi: 10.1186/s12935-021-02263-6</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Nishii K, Satoh Y, Higashi T, et al. Evans Blue and Fluorescein Isothiocyanate-Dextran double labeling reveals precise sequence of vascular leakage and glial responses after exposure to mild-level blast-associated shock waves. J Neurotrauma. 2023;40(11–12):1228–1242. doi: 10.1089/neu.2022.0155</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Mendes NF, Pansani AP, Carmanhães ERF, et al. The blood–brain barrier breakdown during acute phase of the pilocarpine model of epilepsy is dynamic and time-dependent. Front Neurol. 2019;10:382. doi: 10.3389/fneur.2019.00382</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Honeycutt SE, O’Brien LL. Injection of Evans blue dye to fluorescently label and image intact vasculature. Biotechniques. 2021;70(3):181–185. doi: 10.2144/btn-2020-0152</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Salem H, Loux JJ, Smith S, et al. Evaluation of the toxicologic and teratogenic potentials of sodium fluorescein in the rat. Toxicology. 1979;12(2):143–150. doi: 10.1016/0300-483x(79)90040-4</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Acerbi F, Broggi M, Schebesch KM, et al. Fluorescein-guided surgery for resection of high-grade gliomas: a multicentric prospective phase II Study (FLUOGLIO). Clin Cancer Res. 2018;24(1):52–61. doi: 10.1158/1078-0432.CCR-17-1184</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Folaron M, Strawbridge R, Samkoe KS, et al. Elucidating the kinetics of sodium fluorescein for fluorescence-guided surgery of glioma. J Neurosurg. 2018;131(3):724–734. doi: 10.3171/2018.4.JNS172644</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Hawkins BT, Egleton RD. Fluorescence imaging of blood-brain barrier disruption. J Neurosci Methods. 2006;151(2):262–267. doi: 10.1016/j.jneumeth.2005.08.006</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Schoknecht K, Eilers J. Brain-to-blood transport of fluorescein in vitro. Sci Rep. 2024;14(1):25572. doi: 10.1038/s41598-024-77040-2</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Zhang DY, Dmello C, Chen L, et al. Ultrasound-mediated delivery of paclitaxel for glioma: a comparative study of distribution, toxicity, and efficacy of albumin-bound versus cremophor formulations. Clin Cancer Res. 2020;26(2):477–486. doi: 10.1158/1078-0432.CCR-19-2182</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Schaffenrath J, Huang SF, Wyss T, et al. Characterization of the blood–brain barrier in genetically diverse laboratory mouse strains. Fluids Barriers CNS. 2021;18(1):34. doi: 10.1186/s12987-021-00269-w</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Yen LF, Wei VC, Kuo EY, et al. Distinct patterns of cerebral extravasation by Evans blue and sodium fluorescein in rats. PLoS One. 2013;8(7):e68595. doi: 10.1371/journal.pone.0068595</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Poon C, Mühlenpfordt M, Olsman M, et al. Real-time intravital multiphoton microscopy to visualize focused ultrasound and microbubble treatments to increase blood–brain barrier permeability. J Vis Exp. 2022;(180). doi: 10.3791/62235</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>40, Shi L, Zeng M, Sun Y, et al. Quantification of blood–brain barrier solute permeability and brain transport by multiphoton microscopy. J Biomech Eng. 2014;136(3):031005. doi: 10.1115/1.4025892</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Cho EE, Drazic J, Ganguly M, et al. Two-photon fluorescence microscopy study of cerebrovascular dynamics in ultrasound-induced blood-brain barrier opening. J Cereb Blood Flow Metab. 2011;31(9):1852–1862. doi: 10.1038/jcbfm.2011.59</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Barr JL, Brailoiu GC, Unterwald EM, et al. Assessment of blood–brain barrier permeability using miniaturized fluorescence microscopy in freely moving rats. Methods Mol Biol. 2021;2367:123–135. doi: 10.1007/7651_2020_315</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Bricio-Moreno L, Kurt-Jones EA, Sorensen EW, et al. Using multiphoton intravital microscopy to study neutrophil transmigration and blood–brain barrier permeability in a mouse model of herpes simplex virus encephalitis. Methods Mol Biol. 2024;2828:45–55. doi: 10.1007/978-1-0716-4023-4_5</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Nyúl-Tóth Á, Tarantini S, DelFavero J, et al. Demonstration of age-related blood-brain barrier disruption and cerebromicrovascular rarefaction in mice by longitudinal intravital two-photon microscopy and optical coherence tomography. Am J Physiol Heart Circ Physiol. 2021;320(4):H1370–H1392. doi: 10.1152/ajpheart.00709.2020</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Ergin A, Wang M, Zhang JY, et al. The feasibility of real-time in vivo optical detection of blood–brain barrier disruption with indocyanine green. J Neurooncol. 2012;106(3):551–560. doi: 10.1007/s11060-011-0711-5</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Ador T, Fournié M, Rigollet S, et al. Ultrasound-assisted blood-brain barrier opening monitoring by photoacoustic and fluorescence imaging using indocyanine green. Ultrasound Med Biol. 2025;51(7):1059–1069. doi: 10.1016/j.ultrasmedbio.2025.02.016</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Tong S, Liu H, Huang J, et al. In vivo three-photon fluorescence imaging of mouse brain vasculature labeled by Evans blue excited at the NIR-III window. Biomed Opt Express. 2024;16(1):257–266. doi: 10.1364/BOE.545987</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Lee S, Lim W, Ryu HW, et al. ZW800-1 for assessment of blood–brain barrier disruption in a photothrombotic stroke model. Int J Med Sci. 2017;14(13):1430–1435. doi: 10.7150/ijms.22294</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Yu X, Feng Z, Cai Z, et al. Deciphering of cerebrovasculatures via ICG-assisted NIR-II fluorescence microscopy. J Mater Chem B. 2019;7(42):6623–6629. doi: 10.1039/c9tb01381d</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Zhu HJ, Sun YY, Du Y, et al. Albumin-seeking near-infrared-II probe evaluating blood–brain barrier disruption in stroke. J Nanobiotechnology. 2024;22(1):742. doi: 10.1186/s12951-024-02973-9</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Chen S, Chen H, Li X, et al. Dynamic pathophysiological insight into the brain by NIR-II imaging. Adv Sci (Weinh). 2025;12(16):e2416390. doi: 10.1002/advs.202416390</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Barbora A, Bohar O, Sivan AA, et al. Higher pulse frequency of near-infrared laser irradiation increases penetration depth for novel biomedical applications. PLoS One. 2021;16(1):e0245350. doi: 10.1371/journal.pone.0245350</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Aghigh A, Bancelin S, Rivard M, et al. Second harmonic generation microscopy: a powerful tool for bio-imaging. Biophys Rev. 2023;15(1):43-70. doi: 10.1007/s12551-022-01041-6</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Sun H, Wang S, Chen J, et al. Label-free second harmonic generation imaging of cerebral vascular wall in local ischemia mouse model in vivo. Neuroscience. 2022;502:10–24. doi: 10.1016/j.neuroscience.2022.08.003</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Esquibel CR, Wendt KD, Lee HC, et al. Second harmonic generation imaging of collagen in chronically implantable electrodes in brain tissue. Front Neurosci. 2020;14:95. doi: 10.3389/fnins.2020.00095</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Ahn SJ, Ruiz-Uribe NE, Li B, et al. Label-free assessment of hemodynamics in individual cortical brain vessels using third harmonic generation microscopy. Biomed Opt Express. 2020;11(5):2665–2678. doi: 10.1364/BOE.385848</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Liu H, Chen X, Deng X, et al. In vivo deep-brain blood flow speed measurement through third-harmonic generation imaging excited at the 1700-nm window. Biomed Opt Express. 2020;11(5):2738–2744. doi: 10.1364/BOE.389662</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Lu FK, Calligaris D, Olubiyi OI, et al. Label-free neurosurgical pathology with stimulated raman imaging. Cancer Res. 2016;76(12):3451–3462. doi: 10.1158/0008-5472.CAN-16-0270</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Uckermann O, Galli R, Tamosaityte S, et al. Label-free delineation of brain tumors by coherent anti-Stokes Raman scattering microscopy in an orthotopic mouse model and human glioblastoma. PLoS One. 2014;9(9):e107115. doi: 10.1371/journal.pone.0107115</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Ji N. The practical and fundamental limits of optical imaging in mammalian brains. Neuron. 2014;83(6):1242–1245. doi: 10.1016/j.neuron.2014.08.009</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Lee BR, Joo KI, Choi ES, et al. Evans blue dye-enhanced imaging of the brain microvessels using spectral focusing coherent anti-Stokes Raman scattering microscopy. PLoS One. 2017;12(10):e0185519. doi: 10.1371/journal.pone.0185519</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Francis AT, Manifold B, Carlson EC, et al. In vivo simultaneous nonlinear absorption Raman and fluorescence (SNARF) imaging of mouse brain cortical structures. Commun Biol. 2022;5(1):222. doi: 10.1038/s42003-022-03166-6</mixed-citation></ref></ref-list></back></article>
