Electronic Stimulator of Lacrimal Gland
Electronic Stimulator of Lacrimal Gland
批准号:
8827350
负责人:
DANIEL V PALANKER
金额:
$46.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-04-01 至 2017-03-31
关键词:
AcuteAdhesivesAdverse effectsAffectAmericanAnimal ModelAnimalsBlindnessCaringCellsChemicalsChronicClinical ResearchComputer SimulationCorneaDevelopmentDisease ProgressionDry Eye SyndromesElectric StimulationElectrodesEngineeringExcessive tearingEyeEye diseasesFDA approvedFilmFrequenciesGeometryGlandGlassHealthHumanImplantInfectionInferiorInflammationLacrimal gland structureNerveOcular orbitOphthalmologistOryctolagus cuniculusOsmolar ConcentrationOutputPatientsPharmaceutical PreparationsPhotophobiaPhysiciansPhysiologic pulsePreparationProductionQuality of lifeRelative (related person)RiskSafetyShapesSymptomsTeaTechnologyTestingTherapeuticTherapeutic EffectTimeTissuesTranslatingbiomaterial compatibilitydesigneffective therapyelectric fieldelectronic stimulatorevaporationeye drynessimprovedintense painocular surfaceresponsetransmission process
中文摘要
描述(由申请人提供):超过2500万美国人患有干眼病(DED),其中300万人患有最严重的形式-一种没有有效治疗的衰弱状况。 病人和医生都迫切需要治疗。 DED的症状包括剧烈疼痛、光敏感、模糊、感染风险增加和可能的视力丧失。 DED中眼表上的泪液体积不足最初是由泪液产生不足或泪液蒸发过度引起的。 泪液量不足导致泪液高渗,引起炎症和神经损伤,导致泪液产生和质量的进行性损失。 RestasisTM是FDA唯一批准的治疗DED的药物,仅增加23%的泪液分泌,因此不会显著减缓或逆转疾病的进展。 我们已经在人类和动物模型中证明,通过对泪腺进行电刺激可以显著增加泪液的产生。 我们假设泪液量的增加可以改善泪膜渗透压、眼表健康、症状,从而改善生活质量。 它也可以逆转疾病的进展。 将通过插入泪腺旁眼眶的射频微刺激器向泪腺输送电流。 刺激器安全无痛地将电流输送到泪腺,恢复泪液分泌。 功率从放置在眼镜腿上的小型RF发射器无线传输到刺激器,或者作为患者太阳穴上的粘合剂贴片。 刺激兔泪腺显示泪液产生较基线显著增加:高达7倍(+600%)。 与基线相比,使用市售外部刺激器的急性临床研究导致重度DED患者的泪液分泌增加3倍(+195%)。 与RestasisTM相比,这是8倍以上的改进。 该项目汇集了工程师和眼科医生的独特组合,以完成泪腺刺激器的开发和评估其有效性和安全性。 我们将研究刺激机制,优化电极几何形状和波形,并在动物模型中评估慢性刺激的生物相容性,安全性和有效性,为将该技术转化为临床研究做准备。
英文摘要
DESCRIPTION (provided by applicant): More than 25 million Americans have Dry Eye Disease (DED) with 3 million suffering from the most severe form - a debilitating condition with no effective treatments. Patients and physicians are desperate for a cure. Symptoms of DED include intense pain, light sensitivity, blurriness, increased risk of infection, and possible visin loss. Insufficient tear volume on the ocular surface in DED is initially caused by insufficient ter production or excessive tear evaporation. Insufficient tear volume results in tear hyperosmolarity, causing inflammation and nerve damage, leading to progressive loss of tear production and quality. RestasisTM - the only FDA approved medication for the treatment of DED, increases tear production by only 23%, and therefore does not significantly slow or reverse progression of the disease. We have demonstrated in both humans and in animal model that tear production can be dramatically increased by electrical stimulation of the lacrimal gland. We hypothesize that increase in tear volume should improve tear film osmolarity, ocular surface health, symptoms and therefore quality of life. It may also reverse the progression of disease. Electric current will be delivered to lacrimal gland via a RF- powered micro-stimulator inserted into the eye orbit next to the lacrimal gland. The stimulator safely and painlessly delivers electrical current to the lacrimal gland, restoring tear production. Power is wirelessly transmitted to the stimulator from a small RF transmitter placed on the temple of glasses, or as an adhesive patch on the patient's temple. Stimulation of lacrimal gland in rabbits demonstrated a dramatic increase in tear production over baseline: up to 7-fold (+600%). Acute clinical study with a commercially available external stimulator resulted in 3-fold (+195%) increase in tear production in patients with severe DED, compared to baseline. This is more than 8-fold improvement compared to RestasisTM. This project brings together a unique combination of engineers and ophthalmologists to complete the development and evaluate the efficacy and safety of the lacrimal gland stimulator. We will study the mechanisms of stimulation, optimize the electrode geometry and waveforms, and assess biocompatibility, safety and efficacy of chronic stimulation in animal model in preparation for translating this technology to clinical studies.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
Electronic enhancement of tear secretion.
电子撕裂分泌的电子增强。
DOI:
10.1088/1741-2560/13/1/016006
发表时间:
2016-02
期刊:
Journal of neural engineering
影响因子:
4
作者:
[Brinton M, Chung JL, Kossler A, Kook KH, Loudin J, Franke M, Palanker D]
通讯作者:
Palanker D
DOI:
10.1167/iovs.16-21362
发表时间:
2017-04-01
期刊:
Investigative ophthalmology & visual science
影响因子:
4.4
作者:
[Brinton M, Kossler AL, Patel ZM, Loudin J, Franke M, Ta CN, Palanker D]
通讯作者:
Palanker D
Electronic photoreceptors for restoration of sight in retinal degeneration
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项目类别:
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资助金额:$68.15万
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财政年份:2023
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依托单位:
Optoretinography: All-optical measures of functional activity in the human retina
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项目类别:
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资助金额:$16.12万
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项目类别:
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Photovoltaic Subretinal Prosthesis with High Pixel Density
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项目类别:
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财政年份:2017
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依托单位:
Electronic Stimulator of Lacrimal Gland
-
批准号:8629749
-
项目类别:
-
资助金额:$46.34万
-
财政年份:2013
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负责人:DANIEL V PALANKER
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依托单位:
Electronic Stimulator of Lacrimal Gland
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批准号:8477525
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项目类别:
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资助金额:$48.39万
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财政年份:2013
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负责人:DANIEL V PALANKER
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依托单位:
High Resolution Optoelectronic Retinal Prosthesis
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批准号:8281581
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项目类别:
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资助金额:$118.38万
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财政年份:2009
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负责人:DANIEL V PALANKER
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依托单位:
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项目类别:
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资助金额:$113.37万
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财政年份:2009
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负责人:DANIEL V PALANKER
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依托单位:
High Resolution Optoelectronic Retinal Prosthesis
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项目类别:
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资助金额:$125.16万
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财政年份:2009
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依托单位:
High Resolution Optoelectronic Retinal Prosthesis
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批准号:8091258
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项目类别:
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资助金额:$118.38万
-
财政年份:2009
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负责人:DANIEL V PALANKER
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依托单位:
High Resolution Optoelectronic Retinal Prosthesis
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批准号:7650780
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项目类别:
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资助金额:$129.71万
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财政年份:2009
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负责人:DANIEL V PALANKER
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ELECTRICAL ALTERNATIVE LASERS INTRAOCULAR MICROSURGERY
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批准号:6260396
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项目类别:
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资助金额:$29.25万
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财政年份:2001
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项目类别:
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资助金额:$23.03万
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财政年份:2001
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LAMMP SEMINAR SERIES
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-
项目类别:
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资助金额:$2.46万
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项目类别:
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资助金额:$2.46万
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依托单位:
Pulsed Electron Avalanche Knife: Intraocular Microsurg.
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资助金额:$34.31万
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依托单位:
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财政年份:1999
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依托单位:
海外基金