8 results about "Swallowing difficulty" patented technology

The application discloses an intelligent medicine box management system based on multi-modal perception and a biomimetic medication assisting technology, a biomimetic medication assisting module including a lifting type medicine support device and an auxiliary swallowing subsystem, the lifting type medicine support device being capable of self-adaptive adjustment in a vertical direction and a horizontal inclination angle to assist a user in completing a medicine taking action, the auxiliary swallowing subsystem providing a quantitative liquid when detecting that the user has swallowing difficulty to assist the user in completing swallowing, a multi-dimensional medication confirming module confirming whether the user truly completes medication taking through a tablet taking verification dimension, a hand movement verification dimension and an oral cavity contact verification dimension, an intelligent decision module dynamically deciding a best medication taking reminding time and a reminding mode according to current situation information of the user collected by a multi-modal perception module and a judgment result of the multi-dimensional medication confirming module, and controlling the biomimetic medication assisting module to perform corresponding auxiliary actions, and the credibility of chronic disease patient medication compliance data and human-computer interaction friendliness are remarkably improved.

The invention relates to the technical field of medicines, in particular to ibuprofen water-free swallowing granules and a preparation method thereof. The ibuprofen water-free swallowing particles are composed of medicine carrying particles and taste modifying particles. The medicine-carrying particles comprise the following components in percentage by weight: 50.0 to 95.0 percent of ibuprofen, 0 to 20.0 percent of disintegrating agent, 0.5 to 25.0 percent of adhesive and 0 to 50.0 percent of filling agent. The invention further discloses a preparation method of the medicine-carrying particles. The mass ratio of the ibuprofen to the disintegrating agent to the adhesive is (80-90): (0-10): (5-20). And the adhesive is selected from a low-melting-point adhesive. The medicine-carrying particles are granulated by a hot-melting granulator and then mixed with the taste-modifying particles. The ibuprofen water-free swallowing granules prepared by the invention are convenient to carry, can be rapidly disintegrated in the oral cavity and rapidly release medicines, enter gastrointestinal tracts along with swallowing actions to be absorbed, do not need to be swallowed by water, and are good in medication compliance and particularly suitable for patients with swallowing difficulty to take.

1. Name of the product in this design: Pill swallowing aid. 2. Purpose of this design: To help users, especially children, the elderly, or those with swallowing difficulties, take medication more easily and safely. 3. The key design feature of this product is its shape. 4. The image or photograph that best illustrates the design's key points: a 3D model.

The invention discloses an orally disintegrating tablet and a preparation method thereof, and belongs to the technical field of pharmaceutical preparations. The orally disintegrating tablet comprises 0.5-30 wt% of an active component, 25-35 wt% of an adhesive, 25-65 wt% of a filler and 1-10 wt% of a suspending aid, the active component comprises an antipsychotic raw material medicine and / or an antiepileptic raw material medicine. The void ratio of the orally disintegrating tablet is controlled to be 40-90%, even if the active ingredient is a low-solubility raw material medicine, the orally disintegrating tablet also has the fluffy feeling like puffed food, good taste and pleasant experience, meanwhile, the provided orally disintegrating tablet enables the medicine to be rapidly released in the oral cavity, the disintegration time in the oral cavity is shorter than 5 s, and the orally disintegrating tablet is suitable for oral administration. Compared with the oral cavity disintegration time of about 20s of disintegrating tablets and the oral cavity disintegration time of about 15s of oral soluble films in the prior art, the tablet has remarkable advantages, improves the compliance of patients, and greatly reduces the possibility of Tibetan medicine and vomiting of the patients especially for patients with dysphagia.

The invention relates to an anterior cervical plate (10) comprising receiving openings (12, 12*) for bone screws. In order to give the anterior cervical plate, with a locking option for inserted bone screws, an optimized anatomical design in order to reduce swallowing difficulties and tissue irritations, the cervical plate (10) with a normal thickness DN, i.e. the raw thickness of the plate without processing surfaces, tapers beginning at least at its cranial end portion (AE) at a distance AK from a cranial peripheral edge (60), for which the following applies: 0.5 x DN ≤ AK ≤ 3 x DN, preferably 1 x DN ≤ AK ≤ 2.5 x DN on the basis of a Cartesian coordinate system with an X-axis in the longitudinal direction, a Y-axis in the transverse direction and a Z-axis in the thickness direction of the plate (10) in the direction of its thickness extension up to an edge-side rounding section (RA) to 25% to 80% of the normal thickness DN. The tapering of the anterior cervical plate in the transverse direction takes place via a rounding starting from approximately the centre of the bores up to the end of the plate.

The invention provides azithromycin water-free swallowing granules and a preparation method thereof, and belongs to the field of pharmaceutical preparations. The azithromycin water-free swallowing granules are prepared by mixing medicine-containing taste-masking pellets and taste-modifying granules. The medicine-containing taste-masking pellet sequentially comprises a medicine-containing pellet core, an isolating layer and a taste-masking layer from inside to outside, and the medicine-containing pellet core is prepared through a centrifugal pelleting process. The technical problem to be solved is that the azithromycin water-free swallowing granule can realize water-free rapid swallowing, keeps good taste in the whole process, remarkably improves medication convenience and patient compliance, and is particularly suitable for children and other groups with difficulty in swallowing.

An anterior cervical plate (10) with receiving openings (12, 12*) for bone screws is described. To give the anterior cervical plate with locking option for inserted bone screws an optimized anatomical design to reduce swallowing difficulties and tissue irritation, the cervical plate (10) with a normal thickness DN, i.e., the raw thickness of the plate without machined surfaces, tapers at least at its cranial end section (AE) starting at a distance AK from a cranial edge (60), for which the following applies: 0.5 × DN ≤ AK ≤ 3 × DN, preferably 1 × DN ≤ AK ≤ 2.5 × DN Based on a Cartesian coordinate system with an X-axis in the longitudinal direction, a Y-axis in the transverse direction, and a Z-axis in the thickness direction of the plate (10) in the direction of its thickness extension up to an edge-side rounding section (RA) at 25% to 80% of the normal thickness DN. The tapering of the anterior cervical plate in the transverse direction is achieved by a rounding starting from approximately the center of the bores to the end of the plate.

The invention discloses a tablet containing valsartan and an SGLT-2 inhibitor and a preparation method of the tablet, and the tablet is prepared from the following components in parts by weight: 90-165 parts of valsartan, 7-24 parts of the SGLT-2 inhibitor, 115-1250 parts of microcrystalline cellulose and mannitol co-treatment substance, 1.5-5 parts of a lubricant and 11-20 parts of a disintegrating agent. According to the tablet containing the valsartan and the SGLT-2 inhibitor provided by the invention, the valsartan and the SGLT-2 inhibitor are prepared into the compound tablet, so that the medication frequency of a patient can be reduced, a treatment scheme is simplified, and the compliance of the patient can be improved, especially for elderly patients or groups with dysphagia.