Fast Dissolving(빠른 용해)란 무엇입니까?
Fast Dissolving 빠른 용해 - Fast dissolving, chewable tablets, and other orally administered dosage forms consist of super-disintegrating agents which shows rapid and quick action. [1] Keywords: Orodispersible tablet, migraine, sumatriptan, super disintegrate, fast dissolving. [2] Mannitol granules containing Irbesartan nanocrystals were fast dissolving (i. [3] From the aspect of molecular structure, it is discussed how to obtain FRs with the characteristics of salt-tolerant, fast dissolving, low reservoir damage, proper viscosity, environmental friendly and low cost by optimizing molecular structure, charge type and distribution, block mode, and synthesis process. [4]속용성, 씹을 수 있는 정제 및 기타 경구 투여 제형은 신속하고 신속한 작용을 나타내는 초붕해제로 구성된다. [1] 키워드: 구강분산정, 편두통, 수마트립탄, 초붕해, 속용성. [2] Irbesartan 나노결정을 함유하는 만니톨 과립은 빠르게 용해되었다(i. [3] 분자 구조의 측면에서 분자 구조, 전하 유형 및 분포, 블록 모드, 및 합성 과정. [4]
drug delivery system
To reduce these difficulties, the growth of several fast dissolving drug delivery systems has been produced. [1] Introduction: Fast dissolving film technology has been developed out as a alternative drug delivery system that gives an exception advantage for taking medications. [2] In this study, the polymer-free electrospinning was performed in order to produce cyclodextrin/ibuprofen inclusion complex nanofibers, which could have potentials as fast dissolving oral drug delivery system. [3] Fast dissolving tablet (FDT) is one such type of an innovative and unique drug delivery system which is swiftly gaining much attention in the research field of rapid dissolving technology. [4] The concept of fast dissolving drug delivery system emerged from the desire to provide patient with more conventional means of taking their medication. [5]이러한 어려움을 줄이기 위해 몇 가지 빠른 용해 약물 전달 시스템의 성장이 이루어졌습니다. [1] 소개: 속용 필름 기술은 약물 복용에 예외적인 이점을 제공하는 대체 약물 전달 시스템으로 개발되었습니다. [2] nan [3] nan [4] 속용성 약물 전달 시스템의 개념은 환자에게 약물을 복용하는 보다 전통적인 수단을 제공하려는 욕구에서 나왔습니다. [5]
direct compression method
Ibuprofen fast dissolving tablets were formulated employing different superdisintegrants along with the starch glutamate (a novel superdisintegrant) by the direct compression method. [1] Objective: The main aim of the present research work was to formulate fast dissolving tablets of famotidine by direct compression method and to evaluate the effect of synthetic super disintegrating agent on drug release pattern. [2] The aim of the work is an attempt to design, development and evaluation of fast dissolving tablets of Levosalbutamol sulphate by direct compression method with the aid of superdisintegrant addition. [3]이부프로펜 속용정은 직접 압축법에 의해 전분 글루타메이트(새로운 초붕해제)와 함께 다양한 초붕해제를 사용하여 제형화되었습니다. [1] 목적: 본 연구의 주요 목적은 직접압축법에 의한 파모티딘 속용정을 제형화하고, 합성 초붕해제가 약물 방출 패턴에 미치는 영향을 평가하는 것이었다. [2] nan [3]
present research work 현재 연구 작업
The primary objective of the present research work was to develop nanoparticles incorporating (nanoparticulate) fast dissolving (orodispersible) film evincing enhanced solubility and bioavailability of nitrendipine (NIT). [1] Aim: The aims of the present research work was to prepare and characterize the chitosan silicate conjugate, conjugate was included in orally fast dissolving films of levo cetirizine di hydrochloride as a super disintegrant and to compare disintegration efficiency with commercial super disintegrant. [2]현재 연구 작업의 주요 목적은 니트렌디핀(NIT)의 향상된 용해도 및 생체이용률을 나타내는 (나노미립자) 속용성(구분산성) 필름을 포함하는 나노입자를 개발하는 것이었습니다. [1] 목적: 본 연구의 목적은 초붕해제로 levo cetirizine di 염산염의 경구 속용 필름에 포함된 키토산 실리케이트 접합체를 제조하고 특성화하고 붕해 효율을 상용 초붕해제와 비교하는 것이었습니다. [2]
solvent casting method 용제 주조법
A total of nine formulations of fast dissolving films of Losartan Potassium were developed by solvent casting method using film forming polymers such as HPMC E5, E15 and E50 and other film modifiers. [1] The objective of the present research was to prepare fast dissolving orodispersible films (ODFs) for simultaneous administration of BCS class II drug (meloxicam (MX)) and tizanidine (TZ) using solvent casting method to improve the bioavailability of both drugs. [2]필름을 이용한 용제 캐스팅법으로 총 9종의 로자르탄칼륨 속용 필름 제형을 개발하였습니다. HPMC E5, E15 및 E50 및 기타 필름 개질제와 같은 폴리머 형성. [1] 본 연구의 목적은 BCS 클래스 II 약물(멜록시캄(MX))과 티자니딘(TZ)의 동시 투여를 위해 용매 캐스팅 방법을 사용하여 두 약물의 생체이용률을 개선하기 위한 속용성 구강분산 필름(ODF)을 제조하는 것이었습니다. [2]
Formulate Fast Dissolving 빠른 용해 공식화
Hence, an attempt was made to formulate fast dissolving tablets of Rofecoxib. [1] Hence, an attempt was made to formulate fast dissolving tablets of meloxicam. [2] Objective: The present study was aimed to formulate fast dissolving tablets (FDTs) of Aprepitant (APT) using natural and synthetic superdisintegrants with the desired onset of action, increased bioavailability by reducing the frequency of dosage and also reduce the first-pass metabolism of the drug. [3] Objective: The main aim of the present research work was to formulate fast dissolving tablets of famotidine by direct compression method and to evaluate the effect of synthetic super disintegrating agent on drug release pattern. [4] An attempt was made to formulate fast dissolving tablet of Cilnidipine by solid dispersion using melting method with Gelucire 50/13. [5]따라서, Rofecoxib의 속용정을 제형화하려는 시도가 이루어졌다. [1] 따라서, 멜록시캄의 속용정을 제형화하려는 시도가 이루어졌다. [2] 목적: 본 연구는 원하는 작용 개시를 갖는 천연 및 합성 초붕해제를 사용하여 APT(아프레피탄트)의 속용성 정제(FDT)를 제형화하고, 투여 빈도를 감소시켜 생체 이용률을 증가시키며, 또한 초회 통과 대사를 감소시키는 것을 목적으로 하였다. 의약품. [3] 목적: 본 연구의 주요 목적은 직접압축법에 의한 파모티딘 속용정을 제형화하고, 합성 초붕해제가 약물 방출 패턴에 미치는 영향을 평가하는 것이었다. [4] nan [5]
Develop Fast Dissolving
Objectives: To design and develop fast dissolving sublingual films of Granisetron Hydrochloride, with the prime objective to release the drug quickly from the film to facilitate oral absorption. [1] In the present study an attempt has been made to develop fast dissolving tablets (FDT’S) of tramadol hcl using ocimum basilicum gum as natural superdisintegrant to improve disintegration time, dissolution efficacy and patient compliance. [2] The purpose of this study was to develop fast dissolving tablets of Aceclofenac using different concentration of super disintegrants. [3] The aim of the present work is to develop fast dissolving tablets from the solid dispersion of Tenoxicam for enhancement of solubility. [4]목적: 경구 흡수를 촉진하기 위해 필름에서 약물을 신속하게 방출하는 것이 주요 목적으로, Granisetron Hydrochloride의 빠르게 용해되는 설하 필름을 설계 및 개발하는 것입니다. [1] 본 연구에서는 붕해 시간, 용출 효능 및 환자 순응도를 개선하기 위해 천연 초붕해제로 ocimum basilicum 검을 사용하는 트라마돌 hcl의 속용정(FDT's Fast Dissolved Tablet)을 개발하려는 시도가 있었습니다. [2] 본 연구의 목적은 다양한 농도의 초붕해제를 이용한 속용성 아세클로페낙 정제를 개발하는 것이었다. [3] nan [4]
Oral Fast Dissolving 구강 속용해
The concept of oral fast dissolving film is a new weapon of treatment to the remarkable pharmaceutical field over conventional formulation to enhance pharmacological activity and treat intrinsic and extrinsic factors that prevent nausea and vomiting to dissolve rapidly in the tongue. [1] Conclusions & Perspectives: The unique properties of electrospun-medicated nanofibers can be used as oral fast dissolving DDSs of poorly water-soluble drugs. [2] Oral fast dissolving films are novel approach which are used now a days due to better patient compliance, rapid dissolution, onset of action. [3] Combining the advantages of self‐microemulsifying technology and oral fast dissolving technology, a self‐microemulsifying oral fast dissolving films (SMEOFDF) of vitamin D3 was developed in this study. [4]구강 속용성 필름의 개념은 약리 활성을 높이고 오심 및 구토를 방지하는 내인성 및 외인성 인자를 치료하여 혀에서 빠르게 용해되는 기존 제제를 뛰어 넘는 놀라운 제약 분야의 새로운 치료 무기입니다. [1] Conclusions & Perspectives: electrospun-medication nanofibers의 독특한 특성은 난용성 약물의 경구 속용성 DDS로 사용될 수 있습니다. [2] 구강 속용해 필름은 환자의 순응도, 신속한 용출, 작용 개시로 인해 오늘날 사용되는 새로운 접근 방식입니다. [3] 자가 미세유화 기술과 경구 속용해 기술의 장점을 결합하여, 본 연구에서는 비타민 D3의 자가 미세유화 구강 속용성 필름(SMEOFDF)을 개발했습니다. [4]
Evaluate Fast Dissolving
The aim was to formulate and evaluate fast dissolving tablets of diclofenac sodium to improve the bioavailability of the drug and patient compliance. [1] The main objective of this study was to prepare and evaluate fast dissolving tablets of aripiprazole using three different types of superdisintegrants. [2] The aim of the present research work was to prepare and evaluate fast dissolving tablets (FDTs) of fixed dose combination (FDC) of anti-HIV drugs Ritonavir and Lopinavir with a view to enhance patient compliance and minimizes the side effects. [3]목적은 약물의 생체이용률 및 환자 순응도를 개선하기 위해 디클로페낙 나트륨의 속용성 정제를 제형화하고 평가하는 것이었습니다. [1] 이 연구의 주요 목적은 세 가지 유형의 초붕해제를 사용하여 아리피프라졸의 속용정을 제조하고 평가하는 것이었습니다. [2] 현재 연구 작업의 목적은 환자의 순응도를 높이고 부작용을 최소화하기 위해 항HIV 약물인 리토나비르와 로피나비르의 고정 용량 조합(FDC)의 속용성 정제(FDT)를 준비하고 평가하는 것이었습니다. [3]
Prepare Fast Dissolving
The objective of the present research was to prepare fast dissolving orodispersible films (ODFs) for simultaneous administration of BCS class II drug (meloxicam (MX)) and tizanidine (TZ) using solvent casting method to improve the bioavailability of both drugs. [1] Polyvinylpyrrolidone K90 (PVPK90), a water soluble high molecular weight nonionic polymer was processed for the first time with single needle alternating current electrospinning (ACES) and C‐ACES in order to prepare fast dissolving amorphous solid dispersions of spironolactone (SPIR), a poorly water‐soluble antihypertensive model drug. [2] This work aims to prepare fast dissolving oral films (FDOFs) containing nanoparticles of buspirone hydrochloride (BH). [3]본 연구의 목적은 BCS 클래스 II 약물(멜록시캄(MX))과 티자니딘(TZ)의 동시 투여를 위해 용매 캐스팅 방법을 사용하여 두 약물의 생체이용률을 개선하기 위한 속용성 구강분산 필름(ODF)을 제조하는 것이었습니다. [1] 수용성 고분자량 비이온성 고분자인 Polyvinylpyrrolidone K90(PVPK90)은 spironolactone(SPIR)의 속용성 무정형 고체분산체를 제조하기 위해 처음으로 ACES(Single Needle Alternating Current Electrospinning)와 C-ACES로 처리되었다. 수용성 항고혈압 모델 약물. [2] 이 연구는 buspirone hydrochloride(BH)의 나노 입자를 포함하는 속용성 구강 필름(FDOF)을 준비하는 것을 목표로 합니다. [3]
Aceclofenac Fast Dissolving
Objective: To synthesize, characterize and evaluate starch valerate as a superdisintegrant in the formulation of aceclofenac fast dissolving tablets by employing 23 factorial design. [1] Objective: To optimize aceclofenac fast dissolving tablets employing starch glutamate as novel superdisintegrant by 23 Methods: Starch glutamate was prepared by the esterification process. [2]fast dissolving tablet 속용 타블렛
Natural polymers have more preponderant effects on fast dissolving tablets than synthetic polymers. [1] The demands for fast dissolving tablets have received ever increasing day by day during the last decade. [2] Fast dissolving tablets are popular nowadays, as they disintegrated in mouth within a few seconds without using water for swallow. [3] In the course of recent many years, Fast Dissolving Tablets (FDTs) have acquired a lot of consideration as a preferred option in contrast to regular oral dose structures like tablets and containers. [4] Objective: To synthesize, characterize and evaluate starch valerate as a superdisintegrant in the formulation of aceclofenac fast dissolving tablets by employing 23 factorial design. [5] The demands for fast dissolving tablets have received ever increasing day by day during the last 10-15 years for the onset of action. [6] Hence, starch malonate (new superdisintegrant) was prepared and has been evaluated for its superdisintegrant property by incorporating it into fast dissolving tablets of Aceclofenac. [7] The aim was to formulate and evaluate fast dissolving tablets of diclofenac sodium to improve the bioavailability of the drug and patient compliance. [8] Further fast dissolving tablet is prepared to improve bioavailability. [9] Hence, an attempt was made to formulate fast dissolving tablets of Rofecoxib. [10] Objective: To synthesize, characterize and evaluate starch crotonate as a superdisintegrant in the formulation of Piroxicam fast dissolving tablets by employing 23 factorial design. [11] Coprocessing Cyperus esculentus starch and mannitol by fusion (2:1) influenced tablet disintegration and in vitro dissolution and has potential to be used in manufacture of fast dissolving tablet formulations. [12] Hence, an attempt was made to formulate fast dissolving tablets of meloxicam. [13] The present study was focused on preparation and evaluation of Lanzoprazole fast dissolving tablets. [14] However, in certain occurrences as a result of the huge size of dosage forms, and in the uncooperative, pediatric and dysphasia patients, it might make a few problems, to avoid this issues, another type of dosage form is created, which is known as fast dissolving tablet or mouth dissolving tablet. [15] Objective: The present study was aimed to formulate fast dissolving tablets (FDTs) of Aprepitant (APT) using natural and synthetic superdisintegrants with the desired onset of action, increased bioavailability by reducing the frequency of dosage and also reduce the first-pass metabolism of the drug. [16] In the present study an attempt has been made to develop fast dissolving tablets (FDT’S) of tramadol hcl using ocimum basilicum gum as natural superdisintegrant to improve disintegration time, dissolution efficacy and patient compliance. [17] 7%) after 10 min, so it was incorporated in fast dissolving tablets. [18] The best formulation of solid dispersion selected and subjected to fast dissolving tablets. [19] The main objective of this study was to prepare and evaluate fast dissolving tablets of aripiprazole using three different types of superdisintegrants. [20] Ibuprofen fast dissolving tablets were formulated employing different superdisintegrants along with the starch glutamate (a novel superdisintegrant) by the direct compression method. [21] Salah satu pendekatan tersebut adalah pengembangan fast dissolving tablets (FDTs). [22] The purpose of this study was to develop fast dissolving tablets of Aceclofenac using different concentration of super disintegrants. [23] Objectives: To improve the aqueous solubility and dissolution of fexofenadine HCl, an attempt was made to prepare its fast dissolving tablets by lyophilization technique. [24] In solid dosage forms, fast dissolving tablets has proven the best way for ease of administration for the pediatrics and geriatric patients. [25] Methods Formulation of Fast Dissolving Tablets (FDT) is anticipated to provide immediate release of the drug, which in turn, will improve its dissolution profile to provide the initial surge in plasma concentration required in an acute gout attack. [26] The concept of fast dissolving tablet came into existence in late 1970 and further improvements are still going on in connection with its preparation and methodology. [27] Fast dissolving tablets were prepared using dolutegravir sodium solid dispersion, JFS2, and croscarmellose sodium (CCS) in various concentrations using wet granulation technique. [28] RATIONALE: Fast dissolving tablets for sublingual allergen immunotherapy (SLIT) are now globally available and cover the three major allergies grass, house dust mite and ragweed. [29] 5 solid dispersion were selected an taken for formulation of fast dissolving tablet of Ramipril. [30] Therefore, a taste masked generic formulation of 20 mg zinc sulphate fast dissolving tablets with accurate dose and palatable taste was successfully developed and optimized. [31] Objective: The main aim of the present research work was to formulate fast dissolving tablets of famotidine by direct compression method and to evaluate the effect of synthetic super disintegrating agent on drug release pattern. [32] The aim of the present research work was to prepare and evaluate fast dissolving tablets (FDTs) of fixed dose combination (FDC) of anti-HIV drugs Ritonavir and Lopinavir with a view to enhance patient compliance and minimizes the side effects. [33] The aim of the work is an attempt to design, development and evaluation of fast dissolving tablets of Levosalbutamol sulphate by direct compression method with the aid of superdisintegrant addition. [34] The aim of the present work is to develop fast dissolving tablets from the solid dispersion of Tenoxicam for enhancement of solubility. [35] Fast dissolving tablets for all the batches were prepared for in-vitro drug release analysis. [36] The researcher develops a recently fast dissolving tablet (FDT). [37] Fast dissolving tablet (FDT) is one such type of an innovative and unique drug delivery system which is swiftly gaining much attention in the research field of rapid dissolving technology. [38] The concept of formulating fast dissolving tablets containing PCZ offers a suitable and practical approach in serving desired objective of faster disintegration and dissolution characteristics with increased bioavailability. [39] The objective of this study was to investigate differences in the pharmacokinetic patterns between pure drug and an optimized formulation of fast dissolving tablets of Simvastatin. [40] An attempt was made to formulate fast dissolving tablet of Cilnidipine by solid dispersion using melting method with Gelucire 50/13. [41] The current research work was aimed with an objective of formulation development of fast dissolving tablet of montelukast by using co-processed excipient and to evaluate the effect of co-processed excipient over physical mixture of same excipients. [42] SD3 powder was compressed into fast dissolving tablet dosage form. [43] Aim: The main of the study is to formulate and develop orally disintegrating fast dissolving tablet of Metoclopramide hydrochloride. [44] In the present work, fast dissolving tablet of Amlodipine besylate was design with a view to and provide a quick onset of action. [45] Objective: To optimize aceclofenac fast dissolving tablets employing starch glutamate as novel superdisintegrant by 23 Methods: Starch glutamate was prepared by the esterification process. [46]천연 고분자는 합성 고분자보다 속용성 정제에 더 큰 영향을 미칩니다. [1] 속용성 정제에 대한 요구는 지난 10년 동안 날로 증가했습니다. [2] 속용성 정제는 물을 삼키지 않고 입안에서 몇 초 만에 분해되어 요즘 인기가 있습니다. [3] 최근 몇 년 동안 속용성 정제(FDT)는 정제 및 용기와 같은 일반 경구 투여 구조와 달리 선호되는 옵션으로 많은 고려 사항을 획득했습니다. [4] nan [5] 작용 개시에 대한 지난 10-15년 동안 속용성 정제에 대한 요구가 날로 증가하고 있습니다. [6] 따라서, 전분 말로네이트(새로운 초붕해제)가 제조되었고 이를 Aceclofenac의 속용정에 통합하여 초붕해 특성에 대해 평가되었습니다. [7] 목적은 약물의 생체이용률 및 환자 순응도를 개선하기 위해 디클로페낙 나트륨의 속용성 정제를 제형화하고 평가하는 것이었습니다. [8] nan [9] 따라서, Rofecoxib의 속용정을 제형화하려는 시도가 이루어졌다. [10] nan [11] Cyperus esculentus 전분과 만니톨을 융합(2:1)에 의해 공동 처리하면 정제 붕해 및 시험관 내 용해에 영향을 미치며 속용성 정제 제제 제조에 사용될 가능성이 있습니다. [12] 따라서, 멜록시캄의 속용정을 제형화하려는 시도가 이루어졌다. [13] nan [14] 그러나 어떤 경우에는 제형의 거대한 크기로 인해 그리고 비협조적, 소아 및 언어 장애 환자의 경우 몇 가지 문제가 발생할 수 있습니다. 이러한 문제를 피하기 위해 다음과 같은 다른 유형의 제형이 생성됩니다. 빠른 용해 정제 또는 구강 용해 정제. [15] 목적: 본 연구는 원하는 작용 개시를 갖는 천연 및 합성 초붕해제를 사용하여 APT(아프레피탄트)의 속용성 정제(FDT)를 제형화하고, 투여 빈도를 감소시켜 생체 이용률을 증가시키며, 또한 초회 통과 대사를 감소시키는 것을 목적으로 하였다. 의약품. [16] 본 연구에서는 붕해 시간, 용출 효능 및 환자 순응도를 개선하기 위해 천연 초붕해제로 ocimum basilicum 검을 사용하는 트라마돌 hcl의 속용정(FDT's Fast Dissolved Tablet)을 개발하려는 시도가 있었습니다. [17] nan [18] nan [19] 이 연구의 주요 목적은 세 가지 유형의 초붕해제를 사용하여 아리피프라졸의 속용정을 제조하고 평가하는 것이었습니다. [20] 이부프로펜 속용정은 직접 압축법에 의해 전분 글루타메이트(새로운 초붕해제)와 함께 다양한 초붕해제를 사용하여 제형화되었습니다. [21] nan [22] 본 연구의 목적은 다양한 농도의 초붕해제를 이용한 속용성 아세클로페낙 정제를 개발하는 것이었다. [23] nan [24] nan [25] nan [26] nan [27] nan [28] nan [29] nan [30] nan [31] 목적: 본 연구의 주요 목적은 직접압축법에 의한 파모티딘 속용정을 제형화하고, 합성 초붕해제가 약물 방출 패턴에 미치는 영향을 평가하는 것이었다. [32] 현재 연구 작업의 목적은 환자의 순응도를 높이고 부작용을 최소화하기 위해 항HIV 약물인 리토나비르와 로피나비르의 고정 용량 조합(FDC)의 속용성 정제(FDT)를 준비하고 평가하는 것이었습니다. [33] nan [34] nan [35] nan [36] nan [37] nan [38] nan [39] nan [40] nan [41] nan [42] nan [43] nan [44] nan [45] nan [46]
fast dissolving film 속용 필름
A total of nine formulations of fast dissolving films of Losartan Potassium were developed by solvent casting method using film forming polymers such as HPMC E5, E15 and E50 and other film modifiers. [1] The concept of oral fast dissolving film is a new weapon of treatment to the remarkable pharmaceutical field over conventional formulation to enhance pharmacological activity and treat intrinsic and extrinsic factors that prevent nausea and vomiting to dissolve rapidly in the tongue. [2] Aim: The aims of the present research work was to prepare and characterize the chitosan silicate conjugate, conjugate was included in orally fast dissolving films of levo cetirizine di hydrochloride as a super disintegrant and to compare disintegration efficiency with commercial super disintegrant. [3] Six FX fast dissolving films (10 mg FX/ODF), FX1, FX2, FX3, FX4, FX5, and FX6, were prepared by solvent casting technique. [4] Our studies on the performance of formulation development and evaluation of fast dissolving films of Oloptadine HCL its anti-allergic drug. [5] The formulation was optimized by two factors, three levels (32) was used for the formulation optimization of fast dissolving film of Prochlorperazine maleate and experimental trials are performed on all 9 formulation. [6] Introduction: Fast dissolving film technology has been developed out as a alternative drug delivery system that gives an exception advantage for taking medications. [7] In conclusion present study suggested that fast dissolving films has a better ability to cross the sublingual barrier at a faster rate, and hence the delivery system was found to be promising as it has the potential of overcoming the drawbacks associated with tablet formulations available in the market presently. [8] Oral fast dissolving films are novel approach which are used now a days due to better patient compliance, rapid dissolution, onset of action. [9]필름을 이용한 용제 캐스팅법으로 총 9종의 로자르탄칼륨 속용 필름 제형을 개발하였습니다. HPMC E5, E15 및 E50 및 기타 필름 개질제와 같은 폴리머 형성. [1] 구강 속용성 필름의 개념은 약리 활성을 높이고 오심 및 구토를 방지하는 내인성 및 외인성 인자를 치료하여 혀에서 빠르게 용해되는 기존 제제를 뛰어 넘는 놀라운 제약 분야의 새로운 치료 무기입니다. [2] 목적: 본 연구의 목적은 초붕해제로 levo cetirizine di 염산염의 경구 속용 필름에 포함된 키토산 실리케이트 접합체를 제조하고 특성화하고 붕해 효율을 상용 초붕해제와 비교하는 것이었습니다. [3] nan [4] Oloptadine HCL의 항알레르기 약물의 제형 개발 성능 및 속용성 필름 평가에 대한 우리의 연구. [5] 제형은 두 가지 요소에 의해 최적화되었으며, Prochlorperazine maleate의 속용 필름 제형 최적화를 위해 세 가지 수준(32)이 사용되었으며 9개의 제형 모두에 대해 실험적 시도가 수행되었습니다. [6] 소개: 속용 필름 기술은 약물 복용에 예외적인 이점을 제공하는 대체 약물 전달 시스템으로 개발되었습니다. [7] nan [8] 구강 속용해 필름은 환자의 순응도, 신속한 용출, 작용 개시로 인해 오늘날 사용되는 새로운 접근 방식입니다. [9]
fast dissolving oral 빠른 용해 구강
Recent times, fast dissolving oral films were introduced to the market, attracting the attention of a large number of pharmaceutical companies due to their numerous advantages over other oral dosage forms, including ease of administration, better patient compliance, rapid drug absorption, and rapid onset of action with instant bioavailability. [1] Nicotine (NCT), administered in the form of a fast dissolving oral delivery system, can be a potential alternative to nicotine replacement therapy. [2] In this study, Chitosan/pullulan composite nanofiber fast dissolving oral films (FDOFs) were prepared via electrospinning technology. [3] For example, this technique may be employed to produce tablets or fast dissolving oral films (FDFs) with multilayers of active ingredients, which are personalised to patient's needs. [4] This work aims to prepare fast dissolving oral films (FDOFs) containing nanoparticles of buspirone hydrochloride (BH). [5] The fast dissolving oral film were prepared using different polymers like PVA, PVP, HPMC, Carbopol, Pectin and Tragacanth by solvent casting method. [6] In this study, the polymer-free electrospinning was performed in order to produce cyclodextrin/ibuprofen inclusion complex nanofibers, which could have potentials as fast dissolving oral drug delivery system. [7] Fast dissolving oral films provide convenient, safe and simple way of drug administration. [8]최근 속용성 경구용 필름이 시장에 출시되어 다른 경구용 제형에 비해 투여 용이성, 환자 순응도 향상, 빠른 약물 흡수, 빠른 발현 등의 장점으로 많은 제약회사의 주목을 받고 있습니다. 즉각적인 생체 이용률로 작용합니다. [1] 속용성 경구 전달 시스템의 형태로 투여되는 니코틴(NCT)은 니코틴 대체 요법에 대한 잠재적인 대안이 될 수 있습니다. [2] 이 연구에서는 전기방사 기술을 통해 키토산/풀루란 복합 나노섬유 속용성 구강 필름(FDOF)을 제조했습니다. [3] 예를 들어, 이 기술은 환자의 요구에 맞게 개인화되는 활성 성분의 다층으로 정제 또는 속용성 구강 필름(FDF)을 생산하는 데 사용될 수 있습니다. [4] 이 연구는 buspirone hydrochloride(BH)의 나노 입자를 포함하는 속용성 구강 필름(FDOF)을 준비하는 것을 목표로 합니다. [5] nan [6] nan [7] nan [8]
fast dissolving buccal
The present work is mainly focused on preparing fast dissolving buccal films of Curcumin solid dispersion, since Curcumin is a poorly soluble drug. [1] The present work endeavors fabrication of fast dissolving buccal film of clonidine hydrochloride by employing quality by design (QbD) based approach. [2] This study was aimed to formulate DH as fast dissolving buccal films (FDBFs) using a solvent casting method to enhance patient’s compliance. [3] Fast dissolving buccal films are therefore proposed to facilitate this task. [4]Curcumin은 난용성 약물이기 때문에 현재 작업은 주로 Curcumin 고체 분산체의 빠른 용해 협측 필름을 준비하는 데 중점을 두고 있습니다. [1] 현재 작업은 QbD(Quality by Design) 기반 접근 방식을 사용하여 클로니딘 염산염의 빠르게 용해되는 협측 필름 제조에 노력하고 있습니다. [2] 이 연구는 환자의 순응도를 향상시키기 위해 용매 주조 방법을 사용하여 DH를 속용성 협측 필름(FDBF)으로 공식화하는 것을 목표로 했습니다. [3] nan [4]
fast dissolving sublingual 빠른 용해 설하
Objectives: To design and develop fast dissolving sublingual films of Granisetron Hydrochloride, with the prime objective to release the drug quickly from the film to facilitate oral absorption. [1] The aim of present work is to determine and analyse the kinetics of drug release from the fast dissolving sublingual by employing various mathematical models. [2] The drug is found to be absorbed slowly and incompletely from the gastrointestinal tract (oral) bioavailability of the drug is ∼25% in order to increase bio availability lisinopril was formulated as fast dissolving sublingual film A total of 10 formulations of Fast dissolving sublingual film of lisinopril was prepared by using different polymers like HPMC E15, HPMCE5, HPMC E3, HPMC K 15, PVP, PEG 400 as plasticizer, SSG as a super disintegrant. [3]목적: 경구 흡수를 촉진하기 위해 필름에서 약물을 신속하게 방출하는 것이 주요 목적으로, Granisetron Hydrochloride의 빠르게 용해되는 설하 필름을 설계 및 개발하는 것입니다. [1] 현재 작업의 목적은 다양한 수학적 모델을 사용하여 빠르게 용해되는 설하에서 약물 방출의 역학을 결정하고 분석하는 것입니다. [2] nan [3]