Gabapentin (GBP), an antiepileptic and anti-neuropathic agent, suffers from short half-life (5–7 h), has narrow absorption window, and is absorbed via carrier-mediated mechanism resulting in frequent dosing, poor compliance, and poor bioavailability (<60%). Moreover, GBP is a freely water-soluble drug, thus it is considered a challenging candidate to be formulated as extended release dosage form. In this study, raft forming systems were investigated as a potential drug delivery system for prolonging gastric residence time of GBP. A 23 full factorial design was adopted to study the effect of formulation variables (% gellan gum, % GMO, and % LM-pectin 101), on the percent of GBP released at different time intervals (1, 5, and 8 h) as well as ...
For the treatment of gastrointestinal ulcers, raft forming systems incorporating Nizatidine were dev...
A major constraint in oral controlled drug delivery is that not all drug candidates are absorbed uni...
Propranolol hydrochloride, a non-selective β - adrenergic receptor blocking agent, has been widely u...
Gabapentin (GBP), an antiepileptic and anti-neuropathic agent, suffers from short half-life (5–7 h),...
Gabapentin dosage form could be designed to release the drug in the stomach at a rate providing ...
In this work, a fixed-dose combination of gabapentin and flurbiprofen formulated as multilayer table...
Topical delivery of gabapentin is desirable to treat peripheral neuropathic pain conditions whilst a...
Insufficient pharmacokinetic characteristics may be associated with the widespread use of oral dosag...
Oral drug delivery system (DDS) is the preferred route of administration of drugs, but poor bioavail...
Gabapentin is an anticonvulsant which is primarily used to treat peripheral neuropathy. It belongs t...
The development of new drug delivery systems. There are a number of reasons for the intense interest...
The use of floating drug-delivery systems is one method that is used to achieve prolonged gastric re...
Mohamed A El Nabarawi,1 Mahmoud H Teaima,1 Rehab A Abd El-Monem,2 Nagla A El Nabarawy,3 Dalia A Gabe...
For the treatment of gastrointestinal ulcers, raft forming systems incorporating Nizatidine were dev...
Antiparkinsonian drugs, such as Entacapone, must be absorbed in the upper gastrointestinal tract, an...
For the treatment of gastrointestinal ulcers, raft forming systems incorporating Nizatidine were dev...
A major constraint in oral controlled drug delivery is that not all drug candidates are absorbed uni...
Propranolol hydrochloride, a non-selective β - adrenergic receptor blocking agent, has been widely u...
Gabapentin (GBP), an antiepileptic and anti-neuropathic agent, suffers from short half-life (5–7 h),...
Gabapentin dosage form could be designed to release the drug in the stomach at a rate providing ...
In this work, a fixed-dose combination of gabapentin and flurbiprofen formulated as multilayer table...
Topical delivery of gabapentin is desirable to treat peripheral neuropathic pain conditions whilst a...
Insufficient pharmacokinetic characteristics may be associated with the widespread use of oral dosag...
Oral drug delivery system (DDS) is the preferred route of administration of drugs, but poor bioavail...
Gabapentin is an anticonvulsant which is primarily used to treat peripheral neuropathy. It belongs t...
The development of new drug delivery systems. There are a number of reasons for the intense interest...
The use of floating drug-delivery systems is one method that is used to achieve prolonged gastric re...
Mohamed A El Nabarawi,1 Mahmoud H Teaima,1 Rehab A Abd El-Monem,2 Nagla A El Nabarawy,3 Dalia A Gabe...
For the treatment of gastrointestinal ulcers, raft forming systems incorporating Nizatidine were dev...
Antiparkinsonian drugs, such as Entacapone, must be absorbed in the upper gastrointestinal tract, an...
For the treatment of gastrointestinal ulcers, raft forming systems incorporating Nizatidine were dev...
A major constraint in oral controlled drug delivery is that not all drug candidates are absorbed uni...
Propranolol hydrochloride, a non-selective β - adrenergic receptor blocking agent, has been widely u...