291 results about "Prenatal development" patented technology

The invention relates to the technical field of database construction, in particular to a construction method and system for a reproductive medicine database. The method comprises the following steps: acquiring a biological tissue sample of a patient; acquiring reproductive endocrine hormone data, embryo morphological parameter data, immune cell function data and genome variation data from the biological tissue sample of the patient; performing time sequence analysis processing on the hormone fluctuation mode according to the reproductive endocrine hormone data to obtain endocrine dynamic characteristic data; performing image recognition processing based on coherent superposition characteristics of light on the embryo morphological parameter data, and performing embryo development potential evaluation to obtain embryo development potential data; and performing hierarchical clustering processing on the individual heterogeneity of the patient according to the immune cell function data and the genome variation data to obtain immune-genetic typing data of the patient. By means of the quantum dot sensing technology and the multi-channel micro-fluidic chip, standardization of data acquisition is achieved, and the heterogeneity problem of a data source is solved.

The invention belongs to the technical field of light polarization analysis, and discloses a method for determining the sex of an embryo in an egg based on polarization image recognition. Comprising the following steps: acquiring a transmitted spectrum image sequence of a hatching egg to be detected at a plurality of polarization angles, wherein the transmitted spectrum image sequence covers a transmitted spectrum image from visible light to a near-infrared band; extracting a polarization sensitive wave band set of the embryonic tissue according to the polarization state change characteristics of the embryo area in the transmitted spectrum image at different polarization angles; constructing an embryo gender characteristic spectrum based on the polarization degree distribution difference and the spatial texture characteristics of each wave band in the polarization sensitive wave band set; determining an optimal wave band combination for sex determination by analyzing the relevance between a polarization anisotropy index of a specific wave band in the embryo sex characteristic spectrum and an embryo development stage; according to the polarization response mode corresponding to the optimal wave band combination, the sex of the embryo in the egg is judged, and the resource investment and the waiting cost are greatly reduced.

The invention provides a porcine oocyte in-vitro maturation culture solution additive and application thereof, and belongs to the field of embryo engineering, and the additive contains taurine. The additive also contains sodium pyruvate, cysteine, glucose, NaHCO3, fetal calf serum, estradiol, pregnant horse serum gonadotropin and human chorionic gonadotropin. When the porcine oocyte in-vitro maturation culture solution added with the additive is used for culturing porcine oocytes in vitro, the ROS content in the porcine oocytes can be remarkably reduced, the oxidation resistance of the porcine oocytes can be improved, and the mitochondrial distribution of the oocytes can be improved, so that the development of the oocytes can be improved; the maturation of porcine oocytes and the development of early embryos are promoted. When the technology is applied to the pig assisted reproduction technology, the success rate and quality of embryo engineering can be improved; the pig oocyte in-vitro maturation culture solution added with the additive can improve the premature embryo division rate in parthenogenetic activation of the pig oocytes.

The invention provides biopsy liquid and application thereof in pig blastocyst laser cutting, and belongs to the technical field of animal biology. The invention provides a biopsy solution and a preparation method thereof, the biopsy solution can be applied to pig blastocyst biopsy by laser cutting, the problem that at present, no adaptive biopsy solution exists for laser cutting of pig blastocyst is solved, and the invention further provides a method for laser cutting of pig blastocyst by using the biopsy solution. The problems of embryo cell injury, embryo development potential damage and the like possibly caused by laser cutting of the pig blastocyst in the prior art are solved. The biopsy liquid and the use method thereof can be efficiently and accurately applied to acquisition of pig blastocyst trophoblast cells, and are low in cost and good in repeatability.

The invention discloses application of MY-1B in preparation of medicines for improving ovarian aging, belongs to the technical field of biological medicines, and aims to solve the problems of how to effectively delay ovarian aging and improve ovarian functions. Experiments prove that the mRNA m5C modification level of ovarian granular cells in the ovarian aging process is increased, and the expression level of methylated transferase Nsun2 is increased. Ovarian aging caused by mRNA m5C modification level increase can be improved by supplementing the MY-1B, which is embodied in that the MY-1B can reduce the mRNA m5C modification level of aging nest granular cells; the MY-1B can be used for effectively correcting the orbital cycle disorder of the aged ovary and delaying the decline of the ovarian function; the MY-1B plays an important role in reducing the apoptosis level of granulosa cells in senescent ovaries; the MY-1B can improve the storage capacity of ovaries and enhance the quality of oocytes, so that the fertilization rate and the embryonic development potential of the oocytes are improved.

The invention provides application of a sperm tRNA (transfer ribonucleic acid) derived fragment 5 'tRF-Glu-CTC in prediction of development potential of assisted reproductive embryos. The expression of a tRNA derived fragment 5 'tRF-Glu-CTC in a sperm sample is detected, the abnormal expression of the sperm specific tRNA derived fragment 5' tRF-Glu-CTC in a DFI increase patient is verified, and the analysis on the correlation with clinical data and reproductive outcome of the patient prompts that the 5 'tRF-Glu-CTC molecular marker has significant correlation with the reproductive outcome, so that the 5' tRF-Glu-CTC molecular marker can be used for detecting the expression of the sperm specific tRNA derived fragment 5 'tRF-Glu-CTC in the DFI increase patient. The embryonic development potential can be effectively predicted, and a biomarker is provided for assisted reproduction treatment. In different experimental groups, the 5 'tRF-Glu-CTC can significantly improve the prediction precision, and shows good prediction performance in different clinical data. The detection method based on the fragment is expected to become a new tool for evaluating the assisted reproduction curative effect, the reproduction treatment scheme is further optimized, and the success rate is improved.

Methods of enhancing or improving fertility are disclosed. Methods of extending reproductive longevity are disclosed. Methods of increasing oocyte mitochondrial mass or preventing a decrease of oocyte mitochondrial mass are disclosed. Methods of improving embryo development or improving embryo fertilization rate are disclosed. Methods of treating or preventing an ovarian disease or condition are disclosed. Methods of reducing, preventing, or delaying perimenopause, menopause, or a symptom thereof are disclosed. The methods include administering an Emblica extract or a compound constituent of or having a similarity score of at least 95% with a compound constituent of an Emblica extract, or Fucus extract or a compound constituent of or having a similarity score of at least 95% with a compound constituent of a Fucus extract, or a chebula extract or a compound constituent of or having a similarity score of at least 95% with a compound constituent of a chebula extract.

The invention provides an SMMC network-based embryo development quality evaluation method. The method comprises the following steps: inputting embryo images in different development periods; distributing different weights to the embryo image according to the development period, and outputting an attention feature map with channel attention; extracting global features and local features of the attention feature map; fusing the global features and the local features and extracting time sequence features to obtain a spatial-temporal feature map; and inputting the spatial-temporal feature map into a dichotomy full-connection layer for classification, and evaluating the embryonic development quality. By extracting the features in various aspects, the method has more excellent performance in embryo evaluation.

The invention relates to an N2B27 culture medium for inducing generation of bidirectional pluripotent stem cells, one of LY2090314, AS1842856 or CHIR99021 is added into an N2B27 basal culture medium, and the concentration of the CHIR99021 is 10 mu M. The invention also relates to a preparation method of the N2B27 culture medium. The weight of the LY2090314 is 10 nM, and the weight of the AS1842856 is 0.6 [mu] M. The invention also provides an application of the culture medium in induced production of bidirectional pluripotent stem cells. According to the invention, a novel stem cell culture condition for promoting co-expression of genes OCT4 and CDX2 by adding small molecules LY2090314 (LY), AS1842856 (AS) and CHIR99021 to inhibit signal channels of FOXO1 and GSK3 is screened out. The culture conditions are simple and convenient, the application range is wide, the cultured cells keep the characteristics of 16-32 cell stages of the embryos, and the development characteristics of the embryos can be efficiently reproduced. Under the condition of not depending on transcription factors, the screened bidirectional pluripotent stem cells (BPSCs) can promote efficient generation of TSC cells and establish a TSC cell line through independent differentiation of a serum culture medium or induced differentiation of a TSC culture medium. The obstacles between early embryo pedigree are broken, and the research on early embryo development is promoted.

The invention relates to a method for evaluating toxicity of spiroxamine by using zebra fish and application of the method, and belongs to the technical field of toxicity detection. According to the method, spiroxamine culture solutions with different concentrations are prepared for culturing zebrafish embryos, embryonic development detection and juvenile fish behavior testing are carried out, embryonic development detection includes hatching rate, heart rate and body length, and juvenile fish behavior testing includes spontaneous movement testing, vortex escape testing, swimming behavior testing, reflex behavior testing and color stimulation testing. According to the method provided by the invention, the toxic effect of spiroxamine on zebra fish embryos and juvenile fishes is systematically and comprehensively evaluated, the intuition and accuracy of spiroxamine toxicity detection are improved, and the method can be applied to evaluating the toxicity of environmental samples containing spiroxamine.

The invention discloses a dairy cow timed insemination method for controlling ovulation time and improving embryo implantation rate, and relates to the technical field of dairy cow breeding. The problems that follicles on ovaries of postpartum cows are not synchronous in development, ovulation time cannot be accurately regulated and controlled, and embryonic development regulation and control after fertilization are lacked are solved. The method mainly comprises the following steps: three times of gonadotropin releasing hormone injection, two times of cloprostenol sodium injection, gonadotropin releasing hormone injection, luteinizing hormone releasing hormone A3 injection, timed artificial semen deposition, and VADE mixed liquid injection. GnRH is used for actively regulating follicular development, 95% or more of the dairy cows are synchronized after 2-3 rounds of starting, then timing insemination is performed, the conception rate of the postpartum dairy cows can be remarkably increased, compared with the prior art, the pretreatment time is short, the synchronous ovulation rate and conception rate of the dairy cows can be increased, the calving interval is shortened, and the survival rate of the dairy cows is increased. The economic benefit of the pasture is obviously increased, and the breeding management level can be improved on the basis.

The invention provides a trophoblast cell characteristic analysis method and electronic equipment, and relates to the technical field of embryo evaluation. The method comprises the following steps: carrying out space quadrant division on a target blastocyst three-dimensional model obtained by three-dimensional reconstruction to obtain a plurality of sub-quadrants; determining polar trophoblast cell information and wall trophoblast cell information according to the internal cell mass information in each sub-quadrant; determining multiple fusion feature data according to the trophoblast cell information, the polar trophoblast cell information and the wall trophoblast cell information in each sub-quadrant; and according to the fusion feature data and the basic feature data, carrying out embryo development result analysis to obtain estimated development result information of the target blastocyst. According to the scheme, the spatial structure features of the trophoblast cells are fully mined to obtain the fusion features, and the embryonic development result can be analyzed more deeply based on the fusion features, so that the accuracy of embryonic development result evaluation is improved, and clinical selection of embryos with higher development potential is assisted.

The invention relates to the technical field of biomedicine detection reagent manufacturing and reproductive medicine, in particular to an embryonic development potential sperm key protein kit and a use method thereof. The method is characterized in that an antibody combination capable of specifically recognizing a group of key proteins related to embryonic development potential in human sperms is prepared, and the antibodies, a fluorescence labeled secondary antibody, a cell nucleus dye, a concentrated washing liquid, a mounting medium and a pre-coated control porous glass slide are assembled into the special detection kit. The kit can be combined with a multi-mode imaging system (such as a fluorescence / confocal microscope and a common optical microscope) and image analysis software to realize the traditional analysis of sperm morphology and movement ability, and can perform synchronous and accurate qualitative and quantitative analysis with the expression level and subcellular localization of the key protein. The invention provides an integrated molecular detection solution, and provides a powerful tool for sperm quality screening and embryonic development potential prediction in an assisted reproduction technology.

The invention relates to a method for inducing mouse trophoblast stem cells in vitro. According to the method, mouse embryonic stem cells are used as starting cells, Sorcs3 gene knockout mouse embryonic stem cells are obtained through a gene editing technology, and in-vitro induced trophoblast stem cells (iTSCs) are efficiently and rapidly obtained by means of a flow cytometry sorting technology and in combination with specific antibody sorting. According to the invention, the Sorcs3 gene is knocked out from the embryonic stem cell, so that the capability of the embryonic stem cell to differentiate to the trophoblast lineage can be obviously enhanced; an important research platform is provided for deeply researching a lineage intertransformation mechanism of cell masses (ICM) and trophoblast (TE) in the blastocysts, and the method has important significance for researching lineage limitation of early embryonic development of mammals and the like.

A system and method for analyzing mechanical properties of biological tissues combines light-sheet fluorescence microscopy with mechanical perturbation capabilities. The system integrates a MEMS-based compression device, high-speed light-sheet scanner, and digital image correlation analysis to characterize viscoelastic properties of three-dimensional cellular structures. The system enables quantification of spatially-resolved mechanical characteristics and cellular responses through volumetric strain analysis, correlating mechanical properties with fluorescence-based cellular markers. Implementation with maternal-fetal interface models demonstrates capabilities in analyzing tissue mechanics during cellular invasion processes. The system provides applications in studying mechanical interactions in biological processes including embryonic development, cancer metastasis, and wound healing. The disclosed methodology enables unprecedented analysis of mechanical property dynamics at cellular interfaces in three-dimensional tissue environments.

The invention discloses an embryo development stage hierarchical classification method based on a convolutional neural network. The method comprises the following steps: acquiring an embryo image; acquiring a feature map according to the embryo image; fusing the feature maps and carrying out coarseness classification to obtain a main stage probability; fusing the feature maps after coarse granularity classification, and performing fine granularity classification to obtain a sub-stage probability; obtaining a category probability based on the main stage probability and the sub-stage probability; and performing hierarchical classification on the embryonic development stages according to the category probability. The method can improve the classification precision, and reduces the possibility of misclassification.

The invention discloses a bovine oocyte in-vitro maturation culture solution as well as a preparation method and application thereof, and belongs to the technical field of animal reproduction and embryo engineering. The preparation method of the bovine oocyte in-vitro maturation culture solution comprises the step of adding mitoquinine mesylate into a conventional IVM culture solution, wherein the adding concentration of the mitoquinine mesylate is preferably 50 nmol / L. The bovine oocyte in-vitro maturation culture solution provided by the invention can effectively reduce the oxidative stress reaction of the oocytes in the in-vitro culture process, enhance the mitochondrial function and remarkably improve the bovine oocyte in-vitro maturation quality and the embryonic development potential, so that the blastocyst rate is increased, and the problem that the development potential of the existing oocyte IVM culture solution is insufficient is solved.

The presently disclosed subject matter relates to using a haploid inducing line (whether existing or created) and transforming the haploid line so that it encodes cellular machinery capable of editing genes. The transformed haploid inducing line is used as a parent in a cross between two plants. During pollination, the parental gametes fuse to form an embryo; and the gene editing machinery is also delivered to the embryo at this time. During embryonic development, one set of parental chromosomes are lost, and the gene editing machinery operates on the remaining set of chromosomes. Thus, at least one haploid progeny with edited genes is produced from the cross.

This invention relates to the interdisciplinary field of assisted reproductive technology and artificial intelligence, specifically to a system and method for constructing an embryonic developmental trajectory map that integrates morphological features. By deeply integrating static morphological features with dynamic morphodynamic parameters, a more comprehensive panoramic map of embryonic development with richer information dimensions is constructed, overcoming the one-sidedness of single-dimensional assessment. Automated analysis of the map using an AI model reduces the influence of subjective human factors, enabling the discovery of subtle developmental patterns and potential differences that are difficult to discern with the human eye, significantly improving the accuracy of selecting high-quality embryos. The provided developmental trajectory map allows embryologists to intuitively examine the entire developmental process of the embryo and the performance of each key node, enhancing the interpretability and credibility of the assessment process. Through more scientific embryo selection, it is expected to improve embryo implantation and clinical pregnancy rates, and reduce multiple pregnancy and miscarriage rates.

Provided are a reagent combination or a kit for constructing an embryoid and the use thereof. The reagent combination or the kit can be used for inducing a stem cell to produce a blastocyst-like lineage precursor cell, a blastocyst-like cell and / or an embryoid, which are based on small-molecule induction and independent of transgenes, and have a single cell source. The produced blastocyst-like lineage precursor cell and blastocyst-like cell have a full blastocyst lineage, and are seed cells having balanced developmental competence and totipotency, which solves the problem of unbalanced cell maturation in the prior art. The produced embryoid is highly similar to natural embryos in terms of morphological characteristics and transcriptomic characteristics, has the capability of highly reproducing post-implantation embryonic development and / or gastrulation, which is beneficial for research on embryonic development in vitro. The method for inducing the stem cell to produce the blastocyst-like lineage precursor cell, the blastocyst-like cell and / or the embryoid by using the reagent combination or the kit is simple, and has high applicability and high embryoid construction efficiency.

The invention relates to the technical field of embryo quality evaluation, and discloses an embryo development quality evaluation method based on image recognition. The method comprises the following steps: acquiring an embryonic development image sequence, and judging whether the data volume reaches a preset acquisition threshold value; if a threshold value is reached, constructing an embryo feature vector, and processing the embryo feature vector by a multi-dimensional feature dynamic encoder to obtain optimized feature data; a dynamic game-reinforcement learning framework is adopted, and a development quality evaluation strategy is optimized through interaction of an evaluation agent and an embryo population agent; data collaboration is realized by means of a federated learning technology, an abnormal development detection model is trained in a cross-institution mode, embryo abnormal development behaviors are detected based on adversarial training, and an evaluation result is adjusted; and based on a self-adaptive ladder evaluation mechanism, dynamically adjusting an evaluation standard according to embryonic development characteristics and historical records, and calculating a final quality score. The method can comprehensively extract the multi-dimensional dynamic characteristics of the embryo, optimize the evaluation strategy and accurately detect abnormal development.

The present disclosure provides a method for promoting in vitro development of mammalian embryos, comprising the step of adding alpha-ketoglutarate in the embryo development fluid at 90-180h after in vitro fertilization. Compared with the method of adding throughout the whole embryo development, the present disclosure finds that the promotion of embryo development efficiency is more significant when alpha-ketoglutarate is added after 90 hours after fertilization (90 hours to 180 hours after fertilization).

The invention provides an embryonic development evaluation method and device, electronic equipment and a storage medium, and relates to the technical field of assisted reproduction. The method comprises the following steps: acquiring an embryo image of a to-be-evaluated embryo, and extracting an inner cell mass image from the embryo image; traversing the internal cell cluster image, and determining a pixel distribution index corresponding to the internal cell cluster image; determining at least one feature parameter of the internal cell mass image according to a pixel distribution index corresponding to the internal cell mass image; and determining an evaluation result of the to-be-evaluated embryo according to each characteristic parameter of the inner cell mass image. According to the method, pixel traversal is carried out on an extracted internal cell cluster image to obtain position indexes of a plurality of center pixel points so as to obtain a pixel distribution index, and feature mining is carried out based on pixel relative position difference information indicated by the pixel distribution index so as to obtain multiple feature parameters capable of representing texture information of the internal cell cluster image. Therefore, the method is used for evaluating embryonic development, and the accuracy and credibility of an evaluation result are improved.

The invention discloses application of a porphyromonas gingivalis extract in preparation of products related to an embryo cleft palate model, relates to the technical field of molecular biology, and particularly discloses application of the porphyromonas gingivalis extract in construction of the embryo cleft palate model. The research finds that in the embryonic development period, after a porphyromonas gingivalis extract is applied to a parent body by simulating the condition that a periodontitis patient is infected with the porphyromonas gingivalis, a certain probability of cleft palate of an embryo can be caused, and then the application of the porphyromonas gingivalis to construction of related products of an embryo cleft palate model is provided. The invention provides a novel method for constructing a cleft palate embryo, the application field of the porphyromonas gingivalis is expanded, the research on periodontal diseases and systemic toxic and side effects caused by oral infection of the porphyromonas gingivalis is deepened, and a theoretical basis is provided for the occurrence and prevention research of offspring cleft palate of maternal periodontitis patients.

The invention relates to the technical field of biology, and discloses a method for constructing a drosophila embryo permeabilization model, which comprises the following steps: collecting and cleaning drosophila embryos: collecting and washing the drosophila embryos; rinsing the drosophila melanogaster embryos, namely rinsing the drosophila melanogaster embryos by using a bleaching agent solution to remove chorion layers of the drosophila melanogaster embryos, and washing the embryos after rinsing; and performing permeation treatment on the drosophila melanogaster embryo: performing permeation treatment on the drosophila melanogaster embryo without the chorion layer in an embryo permeation solution EPS, and then cleaning in BPS to obtain the drosophila melanogaster embryo permeation model. According to the construction method of the drosophila melanogaster embryo permeabilization model, operation is easy, convenient and rapid, it can be guaranteed that embryo permeability is good, embryo vitality is maintained at the same time, the influence of small molecule drugs on the embryo development process is conveniently studied, and the method is suitable for popularization and application. And favorable conditions are provided for researching cell and molecular mechanisms of embryonic development, toxicological evaluation of small molecular substance screening and screening of related drugs in an embryo model.

The invention belongs to the technical field of bioengineering, and particularly relates to application of RPS26 recombinant protein in promoting early embryonic development of animals. Experiments show that after the RPS26 recombinant protein is added in the early-stage in-vitro embryo culture process of the lamb goats, the blastocyst rate of the lamb goats can be increased to 40.0%; meanwhile, the cell proportion of cell mass in the blastocyst can be remarkably increased, the cell proportion of trophoderm is reduced, and the total number of blastocyst cells is not influenced, so that the blastocyst development rate can be remarkably increased and the blastocyst quality can be improved by utilizing the RPS26 recombinant protein.

The invention discloses an embryo teratogenic substance screening prediction model based on human induced pluripotent stem cells and a construction method thereof, the embryo teratogenic substance screening prediction model is cells and / or cell aggregates, the cells are myocardial cells differentiated from the human induced pluripotent stem cells, and the cell aggregates are embryoid bodies. The embryo teratogenic substance screening prediction model uses human induced pluripotent stem cells to more accurately simulate the environment of human early embryonic development, avoids species difference of animal models, provides a relatively rapid and accurate screening platform, is suitable for high-throughput drug screening, and has good application prospects. Compared with the prior art, the kit has higher sensitivity and specificity, is helpful for eliminating compounds with potential reproductive toxicity in the early stage of drug development, and reduces the risk of later clinical test failure.

To provide a method for culturing avian embryos outside the eggshell that can reliably achieve high embryo survival rates and low embryonic developmental abnormality rates, and that is relatively easy to perform, as well as a method for evaluating the toxicity of test substances using such a culture method. [Solution] The embryo and yolk are removed from the fertilized bird egg and transferred together with avian aqueous oocyte white into a roughly cylindrical well in a culture vessel. The opening of the well, which is filled with avian aqueous oocyte white, is then covered with a porous membrane, and the avian embryo is cultured by turning it over. Preferably, the cultured avian embryo is further cultured in a roughly cylindrical well in which a porous membrane is provided along the inner circumference, and the amount of avian aqueous oocyte white is adjusted so that there is a space between the well and the avian yolk below the opening.

The application relates to the technical field of embryo development dynamic evaluation, and discloses an assisted reproduction management method and system. The method comprises the following steps: acquiring continuous biological state records of an in-vitro development cycle; analyzing and generating a biological state multidimensional space-time sequence; performing contour identification and dynamic tracking, and constructing a morphological trajectory; defining anchor points on the trajectory and generating a set of quantitative descriptors; performing space-time registration on the descriptor set and a development stage reference template, and establishing a mapping relationship; recombining the descriptors into a graph structure according to the mapping relationship; performing hierarchical feature mining on the graph structure, and extracting deep development mode features; inputting the deep features into a trajectory simulator to deduce an expected development trajectory; evaluating the expected trajectory, and outputting a development evaluation report. The application realizes continuous dynamic quantification and deep mode mining of the whole embryo development process, and improves the objectivity and prediction accuracy of development evaluation.

The invention relates to the technical field of artificial breeding of wild animals, in particular to an artificial hatching method for green peacocks. The method mainly comprises the steps of breeding cage building, parent selection and matching, hatching egg management, hatching environment control, embryonic development monitoring, hatching management and brooding management modules, and the hatching rate and the nestling survival rate are remarkably increased by simulating the native habitat environment, optimizing the hatching egg treatment process, precisely regulating and controlling hatching parameters and conducting brooding management in stages. According to the method, parents are screened by adopting a molecular marker technology, inbreeding mating is avoided, and the problem of embryo heat stress is relieved by innovatively combining egg cooling operation. The system is suitable for protecting endangered wild animals and provides a reference example for artificial breeding of rare pheasants.