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小動(dòng)物肺部液體霧化給藥器

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大小鼠氣管內(nèi)定量給藥裝置可輸送定量的氣溶膠到大鼠、小鼠氣管內(nèi)和肺內(nèi),為定量化給藥提供了更好的方案,給藥快捷、操作方便。
公眾號(hào)
產(chǎn)品詳情

肺部液體霧化給藥上海玉研儀器專門為小鼠、大鼠、豚鼠等小動(dòng)物研發(fā)設(shè)計(jì),可精確對(duì)氣管內(nèi)進(jìn)行霧化給藥的裝置??蓪⒍恳后w通過集成在不銹鋼毛細(xì)插管中的氣溶膠霧化微噴頭霧化,毛細(xì)插管可深入動(dòng)物至支氣管分叉處,實(shí)現(xiàn)氣管內(nèi)定量霧化成氣溶膠給藥。相較于傳統(tǒng)口服或注射給藥,藥物可直接作用于肺部,適用于肺部生理、病理、藥理學(xué)研究。



優(yōu)勢(shì)特點(diǎn):

1.適用于小鼠、大鼠、豚鼠、兔子等小動(dòng)物,也可定制大動(dòng)物款
2.氣管內(nèi)直接給藥,無首關(guān)消除,藥物全身效應(yīng)小
3.微量精確給藥,藥物用量可達(dá)25μL(液體)
4.可用于溶液、小細(xì)胞懸浮液、均質(zhì)懸濁液、粘度較低的乳濁液等給藥
5.90%藥物霧化直徑≤30μm(液體),可達(dá)終末細(xì)支氣管甚至呼吸性細(xì)支氣管,可均勻分布于大小鼠肺部組織中
6.使用方便,安全穩(wěn)定,采用不銹鋼材質(zhì),堅(jiān)固穩(wěn)定耐腐蝕
7.具有至少30篇高影響因子SCI文獻(xiàn)發(fā)表,可提供至少1篇IF大于35分的SCI文獻(xiàn)
8.設(shè)備具有CE認(rèn)證證書或EC符合性證書
9.可用于吸入毒理學(xué)、空氣生物學(xué)、生物危害測(cè)試、吸入免疫、吸入治*、藥物研究、環(huán)境評(píng)價(jià)、危害評(píng)估和醫(yī)學(xué)防護(hù)等多領(lǐng)域


應(yīng)用領(lǐng)域:

1. 研究肺部吸收機(jī)制:通過給予標(biāo)記的藥物,可以觀察藥物在肺泡和肺間質(zhì)中的吸收和轉(zhuǎn)運(yùn)過程,也可以準(zhǔn)確測(cè)定藥物在肺泡、肺間質(zhì)等不同部位的吸收速率和吸收程度,從而建立可靠的藥物吸收模型。

2. 分析肺部代謝過程 :使用肺部給藥技術(shù),可以檢測(cè)給藥后藥物在肺內(nèi)代謝產(chǎn)物的形成和變化,幫助分析肺部代謝酶的活性和代謝途徑,也可以分析藥物在肺內(nèi)的代謝動(dòng)力學(xué),包括代謝速率、代謝產(chǎn)物的形成和清理。

3. 評(píng)估肺部清理機(jī)制:肺部給藥可作用于肺部,研究肺泡巨噬細(xì)胞、肺表面活性物質(zhì)、纖毛運(yùn)動(dòng)等對(duì)藥物清理的影響。

4. 探索肺部免疫反應(yīng)和屏障功能:通過肺部給予免疫刺激藥物,可以觀察肺部免疫細(xì)胞的激*和炎癥反應(yīng)。使用標(biāo)記的粒子或大分子作為探針,可以評(píng)估肺血管內(nèi)皮、上皮等屏障結(jié)構(gòu)對(duì)物質(zhì)通透性的調(diào)控作用。

5.建立肺部-全身循環(huán)的藥動(dòng)學(xué)模型:通過肺部給藥數(shù)據(jù),可以建立詳細(xì)的肺部-血漿-全身循環(huán)的藥動(dòng)學(xué)模型,更準(zhǔn)確地預(yù)測(cè)藥物在體內(nèi)的吸收、分布、代謝和清理過程。



氣管內(nèi)給藥示意圖


肺纖維化大小鼠模型

傳統(tǒng)經(jīng)典的復(fù)制肺纖維化大小鼠模型方法是通過氣管內(nèi)滴入博萊霉素溶液,其主要方式有兩種:有創(chuàng)氣管切開滴注以及無創(chuàng)經(jīng)口氣管滴注。有創(chuàng)氣管切開滴注會(huì)對(duì)實(shí)驗(yàn)動(dòng)物造成外源性損傷,增加了實(shí)驗(yàn)動(dòng)物失血過多和感*的風(fēng)險(xiǎn),無創(chuàng)經(jīng)口氣管滴注可引起明顯的肺組織損傷與肺纖維化改變,但溶液呈液滴狀進(jìn)入肺內(nèi),其液滴相對(duì)較大,藥物較集中,容易造成動(dòng)物窒息死亡。


無創(chuàng)經(jīng)口氣管內(nèi)霧化給藥則是一種更新、更有效的促進(jìn)藥物肺內(nèi)均勻分布的方法,可以將博萊霉素溶液分散為體積更小的液滴,在氣流的推動(dòng)下,分散的液滴能進(jìn)入各肺葉,并可到達(dá)外周肺組織,因此造成累及各肺葉、出現(xiàn)程度相近的纖維化改變、范圍更彌散的肺組織損傷,更接近人類肺纖維化改變。氣管內(nèi)霧化博萊霉素溶液對(duì)小鼠的創(chuàng)傷小,很少出現(xiàn)窒息的情況,且不需穿刺氣管,減少了動(dòng)物的損傷與痛苦,降低了實(shí)驗(yàn)鼠的死亡率,并且藥物劑量可以準(zhǔn)確控制,實(shí)驗(yàn)結(jié)果重復(fù)性好,可作為復(fù)制肺纖維化大小鼠模型的良好方案。



由于大小鼠肺部疾病模型造模指向性強(qiáng),需要直接將造模藥物均勻輸送到肺組織中。因此包括**模型,肺纖維化模型,急性肺組織損傷模型,病毒感*模型等肺部疾病模型均可使用經(jīng)口氣管內(nèi)霧化給藥造模。


相關(guān)產(chǎn)品推薦:

合適的工具能幫助您更好地完成工作,氣管插管臺(tái)和小動(dòng)物喉鏡是幫助您完成肺部給藥手術(shù)的得力助手,推薦與肺部干粉霧化給藥器配合使用。


氣管插管平臺(tái)

氣管插管平臺(tái)支持小鼠、大鼠等小動(dòng)物在一個(gè)穩(wěn)定舒適的方位開展氣管插管、藥物灌注及其它類似實(shí)驗(yàn)操作??梢愿鶕?jù)需要進(jìn)行不同孔位的固定,進(jìn)行多種操作角度的調(diào)節(jié),滿足不同實(shí)驗(yàn)類型以及實(shí)驗(yàn)動(dòng)物種類的需求。雙面操作模式,使得肺部給藥操作更為流暢順利,可與我公司小動(dòng)物呼吸機(jī)、麻醉機(jī)、肺部定量給藥器、喉鏡等配合使用,也可根據(jù)要求進(jìn)行定制。


CG-02型




CG-04   



CG-06型



小動(dòng)物喉鏡

SR310型小動(dòng)物喉鏡,用于觀察實(shí)驗(yàn)動(dòng)物的喉部等結(jié)構(gòu),以進(jìn)行肺部給藥、經(jīng)口氣管插管等操作,適用于小鼠、大鼠、豚鼠,也可根據(jù)您的要求進(jìn)行定制。采用光纖LED照明系統(tǒng),提供清晰明亮的光線,給觀察喉部、會(huì)厭等結(jié)構(gòu)的操作人員提供了更好的視野。前端為不銹鋼的葉型尖部,可隨時(shí)拆卸或更換。操作柄的形狀符合人體工程學(xué),使操作更舒適方便。


產(chǎn)品特點(diǎn):

1.外殼采用金屬材質(zhì),堅(jiān)固耐用,易清洗                    

2.操作柄的形狀符合人體工程學(xué)的原理,手握舒適 

3.專為大小鼠口腔結(jié)構(gòu)設(shè)計(jì)的特制葉片,解決了因口腔太小難以插管的難題 

4.具有大鼠葉片和小鼠葉片供選擇 

5.葉片采用不銹鋼材質(zhì),很大限度地減少腐蝕,確保耐用 

6.電池采用兩節(jié)5號(hào)電池,方便更換

參考文獻(xiàn):

1.Zhu, Chuanda, et al. "An elastase nanocomplex with metal cofactors for enhancement of target protein cleavage activity and synergistic antitumor effect." Chemical Engineering Journal (2024): 149902.doi:10.1016/j.cej.2024.149902.
2.Zhu, Chuanda, et al. "An elastase nanocomplex with metal cofactors for enhancement of target protein cleavage activity and synergistic antitumor effect." Chemical Engineering Journal (2024): 149902,doi:10.1016/j.cej.2024.149902
3.Sun, Xiaolin et al. “GSTP alleviates acute lung injury by S-glutathionylation of KEAP1 and subsequent activation of NRF2 pathway.” Redox biology vol. 71 (2024): 103116. doi:10.1016/j.redox.2024.103116
4.Han, Meng-Meng et al. “Inhaled nanoparticles for treating idiopathic pulmonary fibrosis by inhibiting honeycomb cyst and alveoli interstitium remodeling.” Journal of controlled release : official journal of the Controlled Release Society vol. 366 (2024): 732-745. doi:10.1016/j.jconrel.2024.01.032
5.Feng, Xin et al. “First magnetic particle imaging to assess pulmonary vascular leakage in vivo in the acutely injured and fibrotic lung.” Bioengineering & translational medicine vol. 9,2 e10626. 29 Nov. 2023, doi:10.1002/btm2.10626
6.Fan, Weiyang et al. “Naringenin regulates cigarette smoke extract-induced extracellular vesicles from alveolar macrophage to attenuate the mouse lung epithelial ferroptosis through activating EV miR-23a-3p/ACSL4 axis.” Phytomedicine : international journal of phytotherapy and phytopharmacology vol. 124 (2024): 155256. doi:10.1016/j.phymed.2023.155256
7.Li, Cheng et al. “Broad neutralization of SARS-CoV-2 variants by an inhalable bispecific single-domain antibody.” Cell vol. 185,8 (2022): 1389-1401.e18. doi:10.1016/j.cell.2022.03.009
8.Liu, Chang et al. “An Inhalable Hybrid Biomimetic Nanoplatform for Sequential Drug Release and Remodeling Lung Immune Homeostasis in Acute Lung Injury Treatment.” ACS nano vol. 17,12 (2023): 11626-11644. doi:10.1021/acsnano.3c02075
9.Peng, Boya et al. “Robust delivery of RIG-I agonists using extracellular vesicles for anti-cancer immunotherapy.” Journal of extracellular vesicles vol. 11,4 (2022): e12187. doi:10.1002/jev2.12187
10.Yang, Guang, et al. "Noncovalent co-assembly of aminoglycoside antibiotics@ tannic acid nanoparticles for off-the-shelf treatment of pulmonary and cutaneous infections." Chemical Engineering Journal 474 (2023): 145703.do:10.1016/j.cej.2023.145703.
11.Santin, Yohan et al. “Inhalation of acidic nanoparticles prevents doxorubicin cardiotoxicity through improvement of lysosomal function.” Theranostics vol. 13,15 5435-5451. 2 Oct. 2023, doi:10.7150/thno.86310
12.Sun, Han et al. “Application of Lung-Targeted Lipid Nanoparticle-delivered mRNA of soluble PD-L1 via SORT Technology in Acute Respiratory Distress Syndrome.” Theranostics vol. 13,14 4974-4992. 4 Sep. 2023, doi:10.7150/thno.86466
13.Yue, Dayong et al. “Diesel exhaust PM2.5 greatly deteriorates fibrosis process in pre-existing pulmonary fibrosis via ferroptosis.” Environment international vol. 171 (2023): 107706. doi:10.1016/j.envint.2022.107706
14.Zhang, Mengjun et al. “Airway epithelial cell-specific delivery of lipid nanoparticles loading siRNA for asthma treatment.” Journal of controlled release : official journal of the Controlled Release Society vol. 352 (2022): 422-437. doi:10.1016/j.jconrel.2022.10.020
15.Gu, Peiyu et al. “Protective function of interleukin-22 in pulmonary fibrosis.” Clinical and translational medicine vol. 11,8 (2021): e509. doi:10.1002/ctm2.509
16.Wu, Lan et al. “Poly(lactide-co-glycolide) Nanoparticles Mediate Sustained Gene Silencing and Improved Biocompatibility of siRNA Delivery Systems in Mouse Lungs after Pulmonary Administration.” ACS applied materials & interfaces vol. 13,3 (2021): 3722-3737. doi:10.1021/acsami.0c21259
17.Tian, Xidong et al. “Pulmonary Delivery of Reactive Oxygen Species/Glutathione-Responsive Paclitaxel Dimeric Nanoparticles Improved Therapeutic Indices against Metastatic Lung Cancer.” ACS applied materials & interfaces vol. 13,48 (2021): 56858-56872. doi:10.1021/acsami.1c16351
18.Lin, Wei-Ting et al. “Modulation of experimental acute lung injury by exosomal miR-7704 from mesenchymal stromal cells acts through M2 macrophage polarization.” Molecular therapy. Nucleic acids vol. 35,1 102102. 14 Dec. 2023, doi:10.1016/j.omtn.2023.102102
19.Yang, Huilin et al. “Triptolide dose-dependently improves LPS-induced alveolar hypercoagulation and fibrinolysis inhibition through NF-κB inactivation in ARDS mice.” Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie vol. 139 (2021): 111569. doi:10.1016/j.biopha.2021.111569
20.Feng, Xin et al. “First magnetic particle imaging to assess pulmonary vascular leakage in vivo in the acutely injured and fibrotic lung.” Bioengineering & translational medicine vol. 9,2 e10626. 29 Nov. 2023, doi:10.1002/btm2.10626
21.Xiao, Xue et al. “SerpinB1 is required for Rev-erbα-mediated protection against acute lung injury induced by lipopolysaccharide-in mice.” British journal of pharmacology vol. 180,24 (2023): 3234-3253. doi:10.1111/bph.16175
22.Su, Ruonan et al. “Venetoclax nanomedicine alleviates acute lung injury via increasing neutrophil apoptosis.” Biomaterials science vol. 9,13 (2021): 4746-4754. doi:10.1039/d1bm00481f
23.Xu, Yingying et al. “PEGylated pH-responsive peptide-mRNA nano self-assemblies enhance the pulmonary delivery efficiency and safety of aerosolized mRNA.” Drug delivery vol. 30,1 (2023): 2219870. doi:10.1080/10717544.2023.2219870
24.Wu, Yanqi et al. “SN50 attenuates alveolar hypercoagulation and fibrinolysis inhibition in acute respiratory distress syndrome mice through inhibiting NF-κB p65 translocation.” Respiratory research vol. 21,1 130. 27 May. 2020, doi:10.1186/s12931-020-01372-6
25.Chen, Huanjie et al. “Enhanced secretion of hepatocyte growth factor in human umbilical cord mesenchymal stem cells ameliorates pulmonary fibrosis induced by bleomycin in rats.” Frontiers in pharmacology vol. 13 1070736. 6 Jan. 2023, doi:10.3389/fphar.2022.1070736


小動(dòng)物肺部液體霧化給藥器小動(dòng)物肺部液體霧化給藥器
小動(dòng)物肺部液體霧化給藥器
小動(dòng)物肺部液體霧化給藥器

小動(dòng)物肺部液體霧化給藥器

分享到微信

×
大小鼠氣管內(nèi)定量給藥裝置可輸送定量的氣溶膠到大鼠、小鼠氣管內(nèi)和肺內(nèi),為定量化給藥提供了更好的方案,給藥快捷、操作方便。
021-35183767
公眾號(hào)
產(chǎn)品詳情

肺部液體霧化給藥上海玉研儀器專門為小鼠、大鼠、豚鼠等小動(dòng)物研發(fā)設(shè)計(jì),可精確對(duì)氣管內(nèi)進(jìn)行霧化給藥的裝置。可將定量液體通過集成在不銹鋼毛細(xì)插管中的氣溶膠霧化微噴頭霧化,毛細(xì)插管可深入動(dòng)物至支氣管分叉處,實(shí)現(xiàn)氣管內(nèi)定量霧化成氣溶膠給藥。相較于傳統(tǒng)口服或注射給藥,藥物可直接作用于肺部,適用于肺部生理、病理、藥理學(xué)研究。



優(yōu)勢(shì)特點(diǎn):

1.適用于小鼠、大鼠、豚鼠、兔子等小動(dòng)物,也可定制大動(dòng)物款
2.氣管內(nèi)直接給藥,無首關(guān)消除,藥物全身效應(yīng)小
3.微量精確給藥,藥物用量可達(dá)25μL(液體)
4.可用于溶液、小細(xì)胞懸浮液、均質(zhì)懸濁液、粘度較低的乳濁液等給藥
5.90%藥物霧化直徑≤30μm(液體),可達(dá)終末細(xì)支氣管甚至呼吸性細(xì)支氣管,可均勻分布于大小鼠肺部組織中
6.使用方便,安全穩(wěn)定,采用不銹鋼材質(zhì),堅(jiān)固穩(wěn)定耐腐蝕
7.具有至少30篇高影響因子SCI文獻(xiàn)發(fā)表,可提供至少1篇IF大于35分的SCI文獻(xiàn)
8.設(shè)備具有CE認(rèn)證證書或EC符合性證書
9.可用于吸入毒理學(xué)、空氣生物學(xué)、生物危害測(cè)試、吸入免疫、吸入治*、藥物研究、環(huán)境評(píng)價(jià)、危害評(píng)估和醫(yī)學(xué)防護(hù)等多領(lǐng)域


應(yīng)用領(lǐng)域:

1. 研究肺部吸收機(jī)制:通過給予標(biāo)記的藥物,可以觀察藥物在肺泡和肺間質(zhì)中的吸收和轉(zhuǎn)運(yùn)過程,也可以準(zhǔn)確測(cè)定藥物在肺泡、肺間質(zhì)等不同部位的吸收速率和吸收程度,從而建立可靠的藥物吸收模型。

2. 分析肺部代謝過程 :使用肺部給藥技術(shù),可以檢測(cè)給藥后藥物在肺內(nèi)代謝產(chǎn)物的形成和變化,幫助分析肺部代謝酶的活性和代謝途徑,也可以分析藥物在肺內(nèi)的代謝動(dòng)力學(xué),包括代謝速率、代謝產(chǎn)物的形成和清理。

3. 評(píng)估肺部清理機(jī)制:肺部給藥可作用于肺部,研究肺泡巨噬細(xì)胞、肺表面活性物質(zhì)、纖毛運(yùn)動(dòng)等對(duì)藥物清理的影響。

4. 探索肺部免疫反應(yīng)和屏障功能:通過肺部給予免疫刺激藥物,可以觀察肺部免疫細(xì)胞的激*和炎癥反應(yīng)。使用標(biāo)記的粒子或大分子作為探針,可以評(píng)估肺血管內(nèi)皮、上皮等屏障結(jié)構(gòu)對(duì)物質(zhì)通透性的調(diào)控作用。

5.建立肺部-全身循環(huán)的藥動(dòng)學(xué)模型:通過肺部給藥數(shù)據(jù),可以建立詳細(xì)的肺部-血漿-全身循環(huán)的藥動(dòng)學(xué)模型,更準(zhǔn)確地預(yù)測(cè)藥物在體內(nèi)的吸收、分布、代謝和清理過程。



氣管內(nèi)給藥示意圖


肺纖維化大小鼠模型

傳統(tǒng)經(jīng)典的復(fù)制肺纖維化大小鼠模型方法是通過氣管內(nèi)滴入博萊霉素溶液,其主要方式有兩種:有創(chuàng)氣管切開滴注以及無創(chuàng)經(jīng)口氣管滴注。有創(chuàng)氣管切開滴注會(huì)對(duì)實(shí)驗(yàn)動(dòng)物造成外源性損傷,增加了實(shí)驗(yàn)動(dòng)物失血過多和感*的風(fēng)險(xiǎn),無創(chuàng)經(jīng)口氣管滴注可引起明顯的肺組織損傷與肺纖維化改變,但溶液呈液滴狀進(jìn)入肺內(nèi),其液滴相對(duì)較大,藥物較集中,容易造成動(dòng)物窒息死亡。


無創(chuàng)經(jīng)口氣管內(nèi)霧化給藥則是一種更新、更有效的促進(jìn)藥物肺內(nèi)均勻分布的方法,可以將博萊霉素溶液分散為體積更小的液滴,在氣流的推動(dòng)下,分散的液滴能進(jìn)入各肺葉,并可到達(dá)外周肺組織,因此造成累及各肺葉、出現(xiàn)程度相近的纖維化改變、范圍更彌散的肺組織損傷,更接近人類肺纖維化改變。氣管內(nèi)霧化博萊霉素溶液對(duì)小鼠的創(chuàng)傷小,很少出現(xiàn)窒息的情況,且不需穿刺氣管,減少了動(dòng)物的損傷與痛苦,降低了實(shí)驗(yàn)鼠的死亡率,并且藥物劑量可以準(zhǔn)確控制,實(shí)驗(yàn)結(jié)果重復(fù)性好,可作為復(fù)制肺纖維化大小鼠模型的良好方案。



由于大小鼠肺部疾病模型造模指向性強(qiáng),需要直接將造模藥物均勻輸送到肺組織中。因此包括**模型,肺纖維化模型,急性肺組織損傷模型,病毒感*模型等肺部疾病模型均可使用經(jīng)口氣管內(nèi)霧化給藥造模。


相關(guān)產(chǎn)品推薦:

合適的工具能幫助您更好地完成工作,氣管插管臺(tái)和小動(dòng)物喉鏡是幫助您完成肺部給藥手術(shù)的得力助手,推薦與肺部干粉霧化給藥器配合使用。


氣管插管平臺(tái)

氣管插管平臺(tái)支持小鼠、大鼠等小動(dòng)物在一個(gè)穩(wěn)定舒適的方位開展氣管插管、藥物灌注及其它類似實(shí)驗(yàn)操作??梢愿鶕?jù)需要進(jìn)行不同孔位的固定,進(jìn)行多種操作角度的調(diào)節(jié),滿足不同實(shí)驗(yàn)類型以及實(shí)驗(yàn)動(dòng)物種類的需求。雙面操作模式,使得肺部給藥操作更為流暢順利,可與我公司小動(dòng)物呼吸機(jī)、麻醉機(jī)、肺部定量給藥器、喉鏡等配合使用,也可根據(jù)要求進(jìn)行定制。


CG-02型




CG-04   



CG-06型



小動(dòng)物喉鏡

SR310型小動(dòng)物喉鏡,用于觀察實(shí)驗(yàn)動(dòng)物的喉部等結(jié)構(gòu),以進(jìn)行肺部給藥、經(jīng)口氣管插管等操作,適用于小鼠、大鼠、豚鼠,也可根據(jù)您的要求進(jìn)行定制。采用光纖LED照明系統(tǒng),提供清晰明亮的光線,給觀察喉部、會(huì)厭等結(jié)構(gòu)的操作人員提供了更好的視野。前端為不銹鋼的葉型尖部,可隨時(shí)拆卸或更換。操作柄的形狀符合人體工程學(xué),使操作更舒適方便。


產(chǎn)品特點(diǎn):

1.外殼采用金屬材質(zhì),堅(jiān)固耐用,易清洗                    

2.操作柄的形狀符合人體工程學(xué)的原理,手握舒適 

3.專為大小鼠口腔結(jié)構(gòu)設(shè)計(jì)的特制葉片,解決了因口腔太小難以插管的難題 

4.具有大鼠葉片和小鼠葉片供選擇 

5.葉片采用不銹鋼材質(zhì),很大限度地減少腐蝕,確保耐用 

6.電池采用兩節(jié)5號(hào)電池,方便更換

參考文獻(xiàn):

1.Zhu, Chuanda, et al. "An elastase nanocomplex with metal cofactors for enhancement of target protein cleavage activity and synergistic antitumor effect." Chemical Engineering Journal (2024): 149902.doi:10.1016/j.cej.2024.149902.
2.Zhu, Chuanda, et al. "An elastase nanocomplex with metal cofactors for enhancement of target protein cleavage activity and synergistic antitumor effect." Chemical Engineering Journal (2024): 149902,doi:10.1016/j.cej.2024.149902
3.Sun, Xiaolin et al. “GSTP alleviates acute lung injury by S-glutathionylation of KEAP1 and subsequent activation of NRF2 pathway.” Redox biology vol. 71 (2024): 103116. doi:10.1016/j.redox.2024.103116
4.Han, Meng-Meng et al. “Inhaled nanoparticles for treating idiopathic pulmonary fibrosis by inhibiting honeycomb cyst and alveoli interstitium remodeling.” Journal of controlled release : official journal of the Controlled Release Society vol. 366 (2024): 732-745. doi:10.1016/j.jconrel.2024.01.032
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7.Li, Cheng et al. “Broad neutralization of SARS-CoV-2 variants by an inhalable bispecific single-domain antibody.” Cell vol. 185,8 (2022): 1389-1401.e18. doi:10.1016/j.cell.2022.03.009
8.Liu, Chang et al. “An Inhalable Hybrid Biomimetic Nanoplatform for Sequential Drug Release and Remodeling Lung Immune Homeostasis in Acute Lung Injury Treatment.” ACS nano vol. 17,12 (2023): 11626-11644. doi:10.1021/acsnano.3c02075
9.Peng, Boya et al. “Robust delivery of RIG-I agonists using extracellular vesicles for anti-cancer immunotherapy.” Journal of extracellular vesicles vol. 11,4 (2022): e12187. doi:10.1002/jev2.12187
10.Yang, Guang, et al. "Noncovalent co-assembly of aminoglycoside antibiotics@ tannic acid nanoparticles for off-the-shelf treatment of pulmonary and cutaneous infections." Chemical Engineering Journal 474 (2023): 145703.do:10.1016/j.cej.2023.145703.
11.Santin, Yohan et al. “Inhalation of acidic nanoparticles prevents doxorubicin cardiotoxicity through improvement of lysosomal function.” Theranostics vol. 13,15 5435-5451. 2 Oct. 2023, doi:10.7150/thno.86310
12.Sun, Han et al. “Application of Lung-Targeted Lipid Nanoparticle-delivered mRNA of soluble PD-L1 via SORT Technology in Acute Respiratory Distress Syndrome.” Theranostics vol. 13,14 4974-4992. 4 Sep. 2023, doi:10.7150/thno.86466
13.Yue, Dayong et al. “Diesel exhaust PM2.5 greatly deteriorates fibrosis process in pre-existing pulmonary fibrosis via ferroptosis.” Environment international vol. 171 (2023): 107706. doi:10.1016/j.envint.2022.107706
14.Zhang, Mengjun et al. “Airway epithelial cell-specific delivery of lipid nanoparticles loading siRNA for asthma treatment.” Journal of controlled release : official journal of the Controlled Release Society vol. 352 (2022): 422-437. doi:10.1016/j.jconrel.2022.10.020
15.Gu, Peiyu et al. “Protective function of interleukin-22 in pulmonary fibrosis.” Clinical and translational medicine vol. 11,8 (2021): e509. doi:10.1002/ctm2.509
16.Wu, Lan et al. “Poly(lactide-co-glycolide) Nanoparticles Mediate Sustained Gene Silencing and Improved Biocompatibility of siRNA Delivery Systems in Mouse Lungs after Pulmonary Administration.” ACS applied materials & interfaces vol. 13,3 (2021): 3722-3737. doi:10.1021/acsami.0c21259
17.Tian, Xidong et al. “Pulmonary Delivery of Reactive Oxygen Species/Glutathione-Responsive Paclitaxel Dimeric Nanoparticles Improved Therapeutic Indices against Metastatic Lung Cancer.” ACS applied materials & interfaces vol. 13,48 (2021): 56858-56872. doi:10.1021/acsami.1c16351
18.Lin, Wei-Ting et al. “Modulation of experimental acute lung injury by exosomal miR-7704 from mesenchymal stromal cells acts through M2 macrophage polarization.” Molecular therapy. Nucleic acids vol. 35,1 102102. 14 Dec. 2023, doi:10.1016/j.omtn.2023.102102
19.Yang, Huilin et al. “Triptolide dose-dependently improves LPS-induced alveolar hypercoagulation and fibrinolysis inhibition through NF-κB inactivation in ARDS mice.” Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie vol. 139 (2021): 111569. doi:10.1016/j.biopha.2021.111569
20.Feng, Xin et al. “First magnetic particle imaging to assess pulmonary vascular leakage in vivo in the acutely injured and fibrotic lung.” Bioengineering & translational medicine vol. 9,2 e10626. 29 Nov. 2023, doi:10.1002/btm2.10626
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