Resumen de: US2021008122A1
0001 The present disclosure provides cell-based compositions for treating diabetes, methods for identifying cells that preferentially differentiate into endoderm cells, and methods for preparing insulin-producing pancreatic cells, as well as related methods of use for treating diseases related to insulin deficiency.
Resumen de: WO2026156219A1
Provided are methods of deriving a cell population containing pericytes and endothelial progenitor cells from a peripheral blood sample containing non-hematopoielic cells, which rely on culture media supplemented with serum and in certain embodiments also lacking epidermal growth factor, methods of editing mammalian peripheral blood-derived pericytes, and cells generated these methods. Also provided are serum-free defined cell media containing PDGF-beta; VEGF-C; a Notch ligand; a fibroblast growth factor; a TGF-beta superfamily member; an insulin agonist; transferrin; a hepatocyte growth factor; and a Wnt antagonist. The serum-free defined cell media can be used to derive and/or culture pericytes.
Resumen de: WO2026154038A1
A computer implemented method of training a machine learning model configured for predicting a hypoglycemic event for a subject is proposed, comprising: i. (126) receiving at least two time series of glucose sensor data, wherein each time series of glucose sensor data comprises a plurality of glucose measurements measured by a glucose monitoring device (112) configured for detecting glucose in a bodily fluid of the subject, wherein a first time series of the two time series of glucose sensor data is measured at least during and/or after being exposed to a first predefined program of glycemic stimuli, and wherein a second time series of the two time series of glucose sensor data is measured at least during and/or after being exposed to a second predefined program of glycemic stimuli, wherein the second predefined program of glycemic stimuli is different from the first predefined program of glycemic stimuli; ii. (128) forming a first training dataset using the first time series and forming a second training dataset using the second time series; iii. (130) training the machine learning model with the first training dataset and the second training dataset.
Resumen de: US20260207098A1
0000 Embodiments of the invention provide amperometric analyte sensors having optimized elements such as interference rejection membranes as well as methods for making and using such sensors. The amperometric analyte sensor apparatus comprises: a base layer; a conductive layer disposed on the base layer and comprising a working electrode; an interference rejection membrane disposed on an electroactive surface of the working electrode, wherein the interference rejection membrane comprises poly(vinyl alcohol) (PVA) polymers crosslinked by an acid crosslinker, wherein the crosslinker is a dicarboxylic acid type monomer or a polymer comprising a carboxylic acid group; and an analyte sensing layer. While embodiments of the innovation can be used in a variety of contexts, typical embodiments of the invention include glucose sensors used in the management of diabetes.
Resumen de: WO2026154262A1
A non-invasive diagnosis system, which comprises: a device for collecting a breath sample from a user, which comprises a mouthpiece; a spectrometer for measuring Volatile Organic Compounds, VOCs, in the breath sample; and a processor, wherein the processor is configured to analyse the measured VOCs using one or more machine learning models for classifying the user, based on one or more combinations of the measured VOCs, as healthy, prediabetic, Type 1 or Type 2 diabetes mellitus.
Resumen de: US20260207087A1
0000 Disclosed herein is a wearable device for continuous glucose monitoring including a housing having a top surface opposite a bottom surface. A portion of the top surface is moveable relative to the bottom surface. The bottom surface has an opening and is configured to secure directly to skin. A puck assembly has a sensor, a wire coupled to the sensor, and a plurality of contacts. A rigid member is configured to move relative to the bottom surface. An engagement member is configured to rotate about an axis. A cutting element is coupled to the engagement member. Displacement of the movable portion of the top surface moves the rigid member into contact with the engagement member. The cutting element rotates through the opening to form an incision in the skin then to a locked position within the housing. The sensor and the wire advance through the opening and into the incision.
Resumen de: WO2026155698A1
Various embodiments of the present invention relate generally to stem cell biology, developmental biology, and regenerative medicine. More particularly, various embodiments relate to methods, compositions, culture systems, and kits for directing the differentiation of human pluripotent stem cells, including human induced pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs), into pancreatic lineage cells such as functional islet-like cells. In further embodiments, the invention relates to populations of pancreatic lineage cells produced by the disclosed methods, as well as their use in disease modelling, drug screening, and cell replacement therapies for metabolic disorders such as diabetes.
Resumen de: WO2026154477A1
The present disclosure is directed to embodiments for an automated insulin delivery (AID) device which includes, inter alia, a housing including an adhesive tape configured, to adhere the housing to the skin of a user via. an adhesive tape. The housing houses at least an insulin pump including a single lumen cannula, a glucose sensor including a sensor probe, a processor, an insertion assembly for inserting the single lumen cannula, and the sensor probe within subcutaneous tissue, and an automated-insulin-delivery algorithm (AIDA). The sensor probe at least partially resides within the single lumen cannula, and the AIDA is configured as computer instructions operating on the processor causing the processor to automatically control insulin delivery by the insulin pump according to glucose levels from subcutaneous tissue based on signals received from the glucose sensor.
Resumen de: US20260209710A1
0000 A cell culture medium is disclosed. The cell culture medium comprises: a species-specific cell culture medium comprising: bFGF of the species, PDGF-BB of the species, and EGF of the species; and serum of the species. Further disclosed is a canine cell culture medium comprising: canine bFGF, canine PDGF-BB, and canine EGF; and canine serum. A composition is described comprising: a medium comprising: basal medium, sodium bicarbonate, HEPES, L-glutamine, L-alanine, Insulin, hydrocortisone, progesterone, Asc-2-p, holo-transferrin; bFGF of the species, PDGF-BB of the species, and EGF of the species; and serum consistent with the cells of the species; MSC cells of the species. A method of producing exosomes is described, the method comprising: expanding mesenchymal stem cells and/or islet cells in culture, the culture and collecting exosomes released by the mesenchymal and/or adipose stem cells in culture.
Resumen de: US20260209815A1
0000 Embodiments of the invention provide amperometric analyte sensors having elements selected to optimize enzymatic activities associated with such sensors including polymers functionalized with enzymatic mediators as well as methods for making and using such sensors. While embodiments of the invention can be used in a variety of contexts, typical embodiments of the invention include glucose or ketone sensors used in the management of diabetes.
Resumen de: US20260211903A1
Integrated glucose monitoring systems, comprising a memory configured to store data relating to at least two glucose measurements of a user, a glucose safe range, and exogenous data. Wherein the at least two glucose measurements of the user are at different time points t1 and t2; a user interface comprising a display; and a processor comprising computer-executable instructions. Wherein the computer-executable instructions determine a rate of change based on the at least two glucose measurements of the user; determine, based on the at least two glucose measurements of the user and the determined rate of change, a projected glucose level at a future time t3; and provide an alarm at the user interface if, based on at least one point of exogenous data, the projected glucose level at future time t3 is outside of the glucose safe range.
Resumen de: WO2026155234A1
The present disclosure provides a culture medium for cell culturing, the culture medium containing a combination of specific components. The present disclosure provides a culture medium which contains a combination of components selected from the group consisting of: (1) a halcinonide component; (2) an ALK4/7 inhibitor or a TGFβ receptor type-1 kinase inhibitor; (3) a BRD7/9 double degradation factor or a BRD7/9 binding molecule (degradation factor); (4) an LATS1/2 inhibitor, a PKA inhibitor, or an AKT1 inhibitor; (5) a CK1/2 inhibitor, an insulin receptor inhibitor, a Tyr kinase inhibitor, a PKA inhibitor or a PKC inhibitor, or an adenosine kinase inhibitor; (6) an E-selectin inhibitor, a VCAM1 inhibitor, or an ICAM1 inhibitor; and (7) an LATS1 inhibitor + an LATS2 inhibitor.
Resumen de: US20260207136A1
0000 A system includes a wearable device and a charger case. The wearable device is configured to be positioned on an ear of a wearer, and includes first and second body portions and a connection member mechanically coupled to each of the first body portion and the second body portion. The first body portion and/or the second body portion includes a processor, a memory, and a sensor set including at least one of a pulse oximeter, a photoplethysmogram (PPG) sensor, an accelerometer, a temperature sensor, a proximity sensor, an ambient light sensor, or a gyroscopic sensor. The memory stores instructions to cause the processor to calculate at least one of a blood oxygen saturation level, a pulse rate, a blood pressure level, a blood flow rate, a cardiac output/rhythm, a blood sugar level, a blood carbon monoxide level, a blood nitrous oxide level, or an electrocardiogram of the wearer.
Resumen de: WO2026155233A1
Provided is a culture medium for culturing cells containing specific components. Provided is a culture medium comprising at least one component selected from a group consisting of (1) halcinonides, (2) ALK4/7 inhibitor or TGFβ receptor type 1 kinase inhibitor, (3) BRD7/9 dual degradation factor or BRD7/9 binding molecule (degradation factor), (4) LATS1/2 inhibitor, PKA inhibitor, or AKT1 inhibitor, (5) CK1/2 inhibitor, insulin receptor Tyr kinase inhibitor, PKA inhibitor, or PKC inhibitor or adenosine kinase inhibitor, (6) E-selectin inhibitor, VCAM1 inhibitor, or ICAM1 inhibitor, and (7) LATS1 inhibitor + LATS2 inhibitor.
Resumen de: US20260209692A1
0000 The present invention relates to a basal medium composition for animal cell culture. The basal medium composition for animal cell culture according to the present invention contains a yeast extract, amino acids, an inorganic salt, and a sugar, wherein the amino acids in the composition include cystine and/or cysteine, and glutamine.
Resumen de: US20260207176A1
0000 A system and method for artificial intelligence (AI)-assisted medical diagnostics. A real-time endoscopic ultrasound (EUS) video stream of a patient's organ, such as the pancreas, is received at a computing device. The EUS video stream comprises a plurality of imaging modalities, including at least grey-scale data and elastography data representing tissue stiffness. One or more processors execute an AI model, which processes the video stream to identify, segment, and characterize a region of interest. A visual output is generated for display on a user interface in real-time, the output comprising the EUS video stream with a graphical overlay that includes a visual indicator delineating the segmented region and a classification label corresponding to the characterization, thereby providing real-time clinical decision support.
Resumen de: WO2026152526A1
Provided is a refrigeration cup for an insulin pen in which an insulin cartridge is arranged. The refrigeration cup comprises a refrigeration assembly, a cold conduction cylinder (500), a cup lid (100), and a cup body (200). The refrigeration assembly comprises a semiconductor refrigeration sheet (401), a heat conduction member (402), and a heat dissipation fan (403). The semiconductor refrigeration sheet (401) comprises a cold end and a hot end, and the hot end is attached to the heat conduction member (402). The cold conduction cylinder (500) comprises a sealed end (501) and an open end (502), and the cold end is attached to the sealed end (501). The cup lid (100) is suitable for accommodating the refrigeration assembly. The sealed end (501) is relatively fixedly connected to the semiconductor refrigeration sheet (401) and/or the cup lid (100). The cup body (200) comprises a cup wall (201) and a heat preservation cavity (202) defined by the cup wall (201). The open end (502) extends into the heat preservation cavity (202), and the cup lid (100) detachably seals the heat preservation cavity (202). The cold conduction cylinder (500) or the heat preservation cavity (202) defines an accommodating space capable of accommodating at most one or two insulin pens. The accommodating space is also suitable for accommodating the insulin cartridge. The diameter of the accommodating space ranges from 20 mm to 50 mm. By means of limiting the size of the cold conduction cylinder (500), por
Resumen de: US20260207096A1
Analyte sensors featuring an enzyme system comprising diaphorase and a NAD-dependent dehydrogenase may be utilized to detect inhibitors of diaphorase, provided that the transfer of electrons to a working electrode is rate-limiting with respect to the diaphorase. Such analyte sensors may comprise a sensor tail comprising at least a first working electrode, a first active area disposed upon a surface of the first working electrode, and an analyte-permeable membrane overcoating at least the first active area. The enzyme system comprises NAD, reduced NAD, or any combination thereof; a NAD-dependent dehydrogenase, such as NAD-dependent glucose dehydrogenase; and diaphorase. Inhibitors of diaphorase that may be detected include, for example, warfarin, dicoumarol, and similar compounds. A second active area may be present to facilitate detection of an analyte differing from the inhibitor of diaphorase.
Resumen de: WO2024250121A2
Provided are computer-implemented methods, systems and devices for generating a type-II (T2DM) diabetic status prediction, including: extracting voice biomarker feature values from the voice sample for predetermined voice biomarker features; determining the T2DM diabetic status prediction for the subject based on the biomarker feature values and the diabetic status prediction model; and outputting the T2DM diabetic status prediction for the subject. Provided are computer-implemented methods, systems and devices for generating a diabetic status model for predicting a T2DM diabetic status, including: diabetic status labels identifying a corresponding diabetic status for training subjects; and voice samples collected from the training subjects at different time points, each of the voice samples associated with a corresponding diabetic status label; determining voice feature values for corresponding voice features for each of the voice samples in the voice samples; and generating the diabetic status model based on the voice samples and the voice feature values.
Resumen de: WO2018039642A1
Compounds of formula I, (I) or enantiomers thereof, metabolites thereof, derivatives thereof, deuterated derivatives thereof, halogenated derivatives thereof, prodrugs thereof, pharmaceutically acceptable salts thereof, N- oxides thereof, or a combination thereof, processes and intermediates for preparation thereof, compositions thereof, and uses thereof, are provided. Pharmaceutical compositions comprising a compound of formula I and a compound of Formula II: (IIa) (IIb) or enantiomers thereof, metabolites thereof, derivatives thereof, deuterated derivatives thereof, prodrugs thereof, pharmaceutically acceptable salts thereof, N-oxides thereof, or a combination thereof. Compositions and methods for improving the efficacy of DEX, or providing beneficial pharmacokinetic effects to DEX, comprising co-administering a compound of formula I or SARPO, and a compound of Formula II or DEX to a subject in need thereof, and dosage forms, drug delivery systems, methods of treatment thereof.
Resumen de: US20260204414A1
Techniques disclosed herein relate to sensor data. In some embodiments, the techniques may involve obtaining sensor data. The techniques may further involve applying, to the sensor data, a machine learning model trained to identify outlier measurements. The techniques may further involve determining, based on output from the machine learning model, that the sensor data corresponds to an outlier measurement. The techniques may further involve blanking the sensor data based on the output.
Resumen de: US20260204390A1
0000 A blood glucose management method, a user interface, and a related apparatus are provided. According to one example of the blood glucose management method, a first meal time can be determined based on historical blood glucose values of a user; a second meal time can be determined based on one or more of the following: a meal time input by the user, a hand movement of the user, and a heart rate of the user; and a third meal time can be determined based on the first meal time and the second meal time, where the third meal time is used to evaluate a blood glucose health status of the user.
Resumen de: US20260198807A1
0000 A light source is tuned to a range of wavelengths selected for relatively high absorption by glucose, while an optical sensor uses a complementary filter that selectively absorbs in the same spectrum. This optical channel, in combination with a separate, unfiltered reference optical channel, supports a calculation of glucose concentration in target tissue based on a ratiometric comparison of measured light intensities. In embodiments, quantum dots or other techniques can be used to tune the optical spectrum of a light source, while glucose or a similarly absorbing material can be embedded in an optical potting material or the like to create a similarly tuned filter for a corresponding optical sensor. The supporting hardware may usefully be deployed in a wearable physiological monitor for continuous monitoring of glucose (or other target molecules) in the tissue of a user.
Resumen de: US20260199601A1
0000 A wearable dual closed-loop insulin delivery system is provided that integrates both a chemical closed-loop and an electronic closed-loop for precise glycemic control. The system includes a continuous glucose monitor (CGM) configured to obtain real-time blood glucose concentrations of a subject, and a glucose-responsive insulin (GRI) delivery device containing a GRI formulation that autonomously modulates its insulin-release rate in response to the subject's glucose levels, thereby forming a chemical closed-loop. The system further includes a controller having one or more computer processors executing a machine-learning adaptive glucose forecasting model with an Encoder-Decoder architecture. The model receives real-time glucose measurements from the CGM, predicts glycemia dynamics for at least a time period (i.e., 30 minute) future interval, and generates dosing-control signals to adjust both insulin-dosing amount and timing, forming an electronic closed-loop. The controller is operatively connected to the CGM and the GRI delivery device, enabling predictive, automated insulin regulation.
Nº publicación: US20260199610A1 16/07/2026
Solicitante:
ZHEJIANG SUNCLOSE TECH CO LTD [CN]
Zhejiang Sunclose Technology CO., LTD.
Resumen de: US20260199610A1
0000 An insulin pen-type syringe refrigeration cup is provided, which is provided with an insulin pen cartridge. The insulin pen-type syringe refrigeration cup includes a refrigeration component, a cold conduction tube, a cup lid, and a cup body. The cold conduction tube defines a storage space that accommodates insulin pens, the storage space is also suitable for accommodating the insulin pen cartridge. A diameter of the cold conduction tube is 20 mm-50 mm. The cold conduction tube includes an avoidance groove. The cup lid is suitable for accommodating the refrigeration component. The cup body includes a cup wall and an insulation chamber. The cup lid can detachably seal the insulation chamber, and the refrigeration component keeps the insulation chamber in a low temperature state. The present disclosure significantly reduces the volume by limiting the size of the cold conduction tube and providing the avoidance groove.