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  1. AU="Yassin, Heba A"
  2. AU="Blight, Colin R"
  3. AU="Tang, Jack"
  4. AU="Michael E. Dorcas"
  5. AU="Oliveira, Fernando Rocha de"
  6. AU="Rossmanith, R."
  7. AU="Xi He"
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  10. AU="Feng, Sheau-Line"
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  13. AU="Elena D. Nosyreva"
  14. AU="Birara, Sunita"
  15. AU=Banegas Matthew P. AU=Banegas Matthew P.
  16. AU="Mendelow, Alexander David"
  17. AU="Pereira, Taci"
  18. AU="Natalie Taylor"
  19. AU="Moradi, Tayebeh"
  20. AU="Ramesh C. Santra"
  21. AU="Selvarajah, Aravinda"
  22. AU="Vaisman, Adva"
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  1. Artikel ; Online: Aceclofenac-Loaded Microspheres Prepared by Vesicular Ionotropic Gelation to Minimize Drug-induced Gastric Ulcers in Rats.

    Yassin, Heba A / Ibrahim, Mohamed A / Abou-Taleb, Heba A

    Current drug metabolism

    2022  Band 23, Heft 4, Seite(n) 329–338

    Abstract: Background: Aceclofenac is a non-steroidal anti-inflammatory drug and a potent analgesic. However, its oral ingestion may cause gastrointestinal problems, including dyspepsia, abnormal pain, nausea, diarrhea, and ulcerative colitis.: Objective: This ... ...

    Abstract Background: Aceclofenac is a non-steroidal anti-inflammatory drug and a potent analgesic. However, its oral ingestion may cause gastrointestinal problems, including dyspepsia, abnormal pain, nausea, diarrhea, and ulcerative colitis.
    Objective: This study aimed to prepare vesicular-based enteric microspheres containing aceclofenac by ionotropic gelation technique to minimize gastric irritation in rats.
    Methods: The micron-size vesicles were prepared by the ionic-orifice gelation method. Three types of vesicularbased microcapsules containing aceclofenac were prepared by employing sodium alginate as the coating material in combination with Eudragit L100, Eudragit S100, and polyvinylpyrrolidone PVP K90. The drug to sodium alginate to polymer ratios were 1:0.5:0.5, 1:1:1, and 1:1.5:1.5, respectively. Gelation of sodium alginate was induced by the dropwise addition of calcium chloride solution (10 % w/v). Aceclofenac-loaded microspheres were evaluated in terms of aceclofenac content and in vitro drug release, and FTIR, DSC, and XRD were used for physicochemical evaluation of some selected formulae. The effects of microencapsulation on aceclofenac-induced ulcerative activity in male Wistar rats were also investigated.
    Results: The results indicated no interaction between aceclofenac and microcapsules forming polymers. In addition, microcapsules formulations M1, M4, and M7 gave maximal protection in acidic pH and optimal release in alkaline pH. The histopathological studies revealed that the reduction of ulceration is evident from the macroscopic and microscopic studies, which showed complete protection of the tissue morphology with no ulcers, indicating the effectiveness of the microcapsules system against aceclofenac-induced gastric ulceration in rats again.
    Conclusion: Ionotropic gelation seems to be a simple, efficient technique to prepare aceclofenac-loaded microspheres with a reduced risk of gastric ulceration. It is possible to overcome the problem of gastric damage while utilizing aceclofenac by avoiding the exposure of the drug to the ulcer-prone area of the gastrointestinal tract.
    Mesh-Begriff(e) Alginates/chemistry ; Animals ; Capsules ; Diclofenac/analogs & derivatives ; Male ; Microspheres ; Polymers/chemistry ; Rats ; Rats, Wistar ; Stomach Ulcer/chemically induced ; Stomach Ulcer/prevention & control
    Chemische Substanzen Alginates ; Capsules ; Polymers ; Diclofenac (144O8QL0L1) ; aceclofenac (RPK779R03H)
    Sprache Englisch
    Erscheinungsdatum 2022-03-22
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ZDB-ID 2064815-7
    ISSN 1875-5453 ; 1389-2002
    ISSN (online) 1875-5453
    ISSN 1389-2002
    DOI 10.2174/1389200223666220321111214
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Fabrication and In Vitro/In Vivo Appraisal of Metronidazole Intra-Gastric Buoyant Sustained-Release Tablets in Healthy Volunteers.

    Elkomy, Mohammed H / Abou-Taleb, Heba A / Eid, Hussein M / Yassin, Heba A

    Pharmaceutics

    2022  Band 14, Heft 4

    Abstract: Helicobacter ... ...

    Abstract Helicobacter pylori
    Sprache Englisch
    Erscheinungsdatum 2022-04-14
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2527217-2
    ISSN 1999-4923
    ISSN 1999-4923
    DOI 10.3390/pharmaceutics14040863
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: Evaluation of Brain Targeting and Antipsychotic Activity of Nasally Administrated Ziprasidone Lipid-Polymer Hybrid Nanocarriers.

    Abo El-Enin, Hadel A / Tulbah, Alaa S / Darwish, Hany W / Salama, Rania / Naguib, Ibrahim A / Yassin, Heba A / Abdel-Bar, Hend Mohamed

    Pharmaceuticals (Basel, Switzerland)

    2023  Band 16, Heft 6

    Abstract: The feasibility of using lipid-polymer hybrid (LPH) nanocarriers as a potential platform for the intranasal delivery of ziprasidone (ZP), a second-generation antipsychotic, was explored. Different ZP-loaded LPH composed of a PLGA core and cholesterol- ... ...

    Abstract The feasibility of using lipid-polymer hybrid (LPH) nanocarriers as a potential platform for the intranasal delivery of ziprasidone (ZP), a second-generation antipsychotic, was explored. Different ZP-loaded LPH composed of a PLGA core and cholesterol-lecithin lipid coat were prepared using a single step nano-precipitation self-assembly technique. Modulation of polymer, lipid and drug amounts, as well as stirring-speed-optimized LPH with a particle size of 97.56 ± 4.55 nm and a ZP entrapment efficiency (EE%) of 97.98 ± 1.22%. The brain deposition and pharmacokinetics studies proved the efficiency of LPH to traverse the blood-brain barrier (BBB) following intranasal delivery with a 3.9-fold increase in targeting efficiency compared to the intravenous (IV) ZP solution with a direct nose-to-brain transport percentage (DTP) of 74.68%. The ZP-LPH showed enhanced antipsychotic activity in terms of animals' hypermobility over an IV drug solution in schizophrenic rats. The obtained results showed that the fabricated LPH was able to improve ZP brain uptake and proved its antipsychotic efficiency.
    Sprache Englisch
    Erscheinungsdatum 2023-06-15
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2193542-7
    ISSN 1424-8247
    ISSN 1424-8247
    DOI 10.3390/ph16060886
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: Quetiapine Albumin Nanoparticles as an Efficacious Platform for Brain Deposition and Potentially Improved Antipsychotic Activity.

    Abdel-Bar, Hend Mohamed / Tulbah, Alaa S / Darwish, Hany W / Salama, Rania / Naguib, Ibrahim A / Yassin, Heba A / Abo El-Enin, Hadel A

    Pharmaceutics

    2023  Band 15, Heft 7

    Abstract: Quetiapine (QP) is a second-generation short-acting antipsychotic drug extensively metabolized in the liver, producing pharmacologically inactive metabolites and leading to diminished bioavailability. Therefore, this study aimed to develop an intravenous ...

    Abstract Quetiapine (QP) is a second-generation short-acting antipsychotic drug extensively metabolized in the liver, producing pharmacologically inactive metabolites and leading to diminished bioavailability. Therefore, this study aimed to develop an intravenous QP albumin nanoparticles (NPs) system for improving QP antipsychotic activity and brain targeting. QP-loaded albumin NPs were prepared by the desolvation method. The fabricated NPs were characterized in terms of particle size, zeta potential, entrapment efficiency (EE%), and in vitro drug release. In vivo pharmacokinetics and biodistribution in rats were studied. In addition, the antipsychotic activity of the optimized platform was also investigated. Human serum albumin (HSA) concentration, pH, and stirring time were modulated to optimize QP albumin NPs with a particle size of 103.54 ± 2.36 nm and a QP EE% of 96.32 ± 3.98%. In addition, the intravenous administration of QP albumin NPs facilitated QP brain targeting with a 4.9-fold increase in targeting efficiency compared to the oral QP solution. The QP albumin NPs improved the QP antipsychotic activity, indicated by suppressing rats' hypermobility and reducing the QP's extrapyramidal side effects. The obtained results proposed that intravenous QP- NPs could improve QP brain targeting and its antipsychotic efficiency.
    Sprache Englisch
    Erscheinungsdatum 2023-06-21
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2527217-2
    ISSN 1999-4923
    ISSN 1999-4923
    DOI 10.3390/pharmaceutics15071785
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Bucco-Adhesive Film as a Pediatric Proper Dosage Form for Systemic Delivery of Propranolol Hydrochloride: In-vitro and in-vivo Evaluation.

    Mohamad, Soad A / Salem, Hesham / Yassin, Heba A / Mansour, Heba F

    Drug design, development and therapy

    2020  Band 14, Seite(n) 4277–4289

    Abstract: Objective: To formulate and assess bucco-adhesive films of propranolol hydrochloride for pediatric use.: Methods: Different films were formulated adopting mucin, polyvinyl alcohol, chitosan and carbopol. A drug/polymer compatibility study was ... ...

    Abstract Objective: To formulate and assess bucco-adhesive films of propranolol hydrochloride for pediatric use.
    Methods: Different films were formulated adopting mucin, polyvinyl alcohol, chitosan and carbopol. A drug/polymer compatibility study was conducted adopting differential scanning calorimetry and Fourier transform infrared spectroscopy. The prepared films were physically investigated for variation of weight, propranolol content, thickness, surface pH, proportion of moisture, folding endurance and mucoadhesion. In vitro drug release study and kinetic analysis of the corresponding data have been conducted. The optimized formulation was selected for a bioavailability study using albino rabbits and adopting a developed HPLC method. The pharmacokinetic parameters of the drug were calculated following administration of the optimized film and the corresponding marketed oral tablets to albino rabbits.
    Key finding: The compatibility study revealed the absence of drug/polymer interaction. The film formulations had suitable mucoadhesive and mechanical properties. The optimized formulation exhibited reasonable drug release that followed Higuchi diffusion pattern. The calculated AUC0-8h presented an enhancement in the bioavailability of propranolol hydrochloride from the selected film formulation by 1.9 times relative to the marketed propranolol oral tablets.
    Conclusion: These findings support that propranolol hydrochloride bucco-adhesive film can be considered as a proper effective dosage form for pediatric delivery.
    Mesh-Begriff(e) Adhesiveness ; Adhesives ; Administration, Buccal ; Adrenergic beta-Antagonists/administration & dosage ; Adrenergic beta-Antagonists/chemistry ; Adrenergic beta-Antagonists/pharmacology ; Animals ; Area Under Curve ; Biological Availability ; Cheek ; Child ; Chromatography, High Pressure Liquid ; Dosage Forms ; Drug Compounding ; Excipients ; Humans ; Hydrogen-Ion Concentration ; Infant ; Propranolol/administration & dosage ; Propranolol/pharmacokinetics ; Propranolol/pharmacology ; Rabbits
    Chemische Substanzen Adhesives ; Adrenergic beta-Antagonists ; Dosage Forms ; Excipients ; Propranolol (9Y8NXQ24VQ)
    Sprache Englisch
    Erscheinungsdatum 2020-10-15
    Erscheinungsland New Zealand
    Dokumenttyp Journal Article
    ZDB-ID 2451346-5
    ISSN 1177-8881 ; 1177-8881
    ISSN (online) 1177-8881
    ISSN 1177-8881
    DOI 10.2147/DDDT.S267317
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Retama monosperma

    Alyami, Mohammad H / Fakhry, Amal M / El Halfawy, Nancy M / Toto, Soliman M / Sedky, Nada K / Yassin, Heba A / Fahmy, Sherif Ashraf / Mokhtar, Fatma A

    RSC advances

    2023  Band 13, Heft 37, Seite(n) 26213–26228

    Abstract: In this study, ...

    Abstract In this study,
    Sprache Englisch
    Erscheinungsdatum 2023-09-04
    Erscheinungsland England
    Dokumenttyp Journal Article
    ISSN 2046-2069
    ISSN (online) 2046-2069
    DOI 10.1039/d3ra05116a
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: Novel nasal niosomes loaded with lacosamide and coated with chitosan: A possible pathway to target the brain to control partial-onset seizures.

    Tulbah, Alaa S / Elkomy, Mohammed H / Zaki, Randa Mohammed / Eid, Hussein M / Eissa, Essam M / Ali, Adel A / Yassin, Heba A / Aldosari, Basmah Nasser / Naguib, Ibrahim A / Hassan, Amira H

    International journal of pharmaceutics: X

    2023  Band 6, Seite(n) 100206

    Abstract: This work aimed to develop and produce lacosamide-loaded niosomes coated with chitosan (LCA-CTS-NSM) using a thin-film hydration method and the Box-Behnken design. The effect of three independent factors (Span 60 amount, chitosan concentration, and ... ...

    Abstract This work aimed to develop and produce lacosamide-loaded niosomes coated with chitosan (LCA-CTS-NSM) using a thin-film hydration method and the Box-Behnken design. The effect of three independent factors (Span 60 amount, chitosan concentration, and cholesterol amount) on vesicle size, entrapment efficiency, zeta potential, and cumulative release (8 h) was studied. The optimal formulation of LCA-CTS-NSM was chosen from the design space and assessed for morphology, in vitro release, nasal diffusion, stability, tolerability, and in vivo biodistribution for brain targeting after intranasal delivery. The vesicle size, entrapment, surface charge, and in vitro release of the optimal formula were found to be 194.3 nm, 58.3%, +35.6 mV, and 81.3%, respectively. Besides, it exhibits sustained release behavior, enhanced nasal diffusion, and improved physical stability. Histopathological testing revealed no evidence of toxicity or structural damage to the nasal mucosa. It demonstrated significantly more brain distribution than the drug solution. Overall, the data is encouraging since it points to the potential for non-invasive intranasal administration of LCA as an alternative to oral or parenteral routes.
    Sprache Englisch
    Erscheinungsdatum 2023-08-12
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ISSN 2590-1567
    ISSN (online) 2590-1567
    DOI 10.1016/j.ijpx.2023.100206
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: COVID-19: Vaccine Delivery System, Drug Repurposing and Application of Molecular Modeling Approach.

    Abd El Hadi, Soha R / Zien El-Deen, Esmat E / Bahaa, Mostafa M / Sadakah, Abdelfattah A / Yassin, Heba A

    Drug design, development and therapy

    2021  Band 15, Seite(n) 3313–3330

    Abstract: The acute respiratory syndrome coronavirus (SARS-CoV-2) has spread across the world, resulting in a pandemic COVID-19 which is a human zoonotic disease that is caused by a novel coronavirus (CoV) strain thought to have originated in wild or captive bats ... ...

    Abstract The acute respiratory syndrome coronavirus (SARS-CoV-2) has spread across the world, resulting in a pandemic COVID-19 which is a human zoonotic disease that is caused by a novel coronavirus (CoV) strain thought to have originated in wild or captive bats in the initial COVID outbreak region. The global COVID-19 outbreak started in Guangdong Province, China's southernmost province. The global response to the COVID-19 pandemic has been hampered by the sheer number of infected people, many of whom need intensive care before succumbing to the disease. The epidemic is being handled by a combination of disease control by public health interventions and compassionate treatment for those who have been impacted. There is no clear anti-COVID-19 medication available at this time. However, the need to find medications that can turn the tide has led to the development of a number of investigational drugs as potential candidates for improving outcomes, especially in the severely and critically ill. Although many of these adjunctive medications are still being studied in clinical trials, professional organizations have attempted to define the circumstances in which their use is deemed off-label or compassionate. It is important to remind readers that new information about COVID-19's clinical features, treatment options, and outcomes is released on a regular basis. The mainstay of treatment remains optimized supportive care, and the therapeutic effectiveness of the subsequent agents is still being studied.
    Mesh-Begriff(e) Animals ; Antiviral Agents/administration & dosage ; Antiviral Agents/chemistry ; COVID-19/epidemiology ; COVID-19/immunology ; COVID-19/virology ; COVID-19 Vaccines/administration & dosage ; COVID-19 Vaccines/chemistry ; Drug Carriers ; Drug Compounding ; Drug Repositioning ; Host-Pathogen Interactions ; Humans ; Models, Molecular ; Nanoparticles ; SARS-CoV-2/drug effects ; SARS-CoV-2/pathogenicity ; Vaccination ; COVID-19 Drug Treatment
    Chemische Substanzen Antiviral Agents ; COVID-19 Vaccines ; Drug Carriers
    Sprache Englisch
    Erscheinungsdatum 2021-07-30
    Erscheinungsland New Zealand
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2451346-5
    ISSN 1177-8881 ; 1177-8881
    ISSN (online) 1177-8881
    ISSN 1177-8881
    DOI 10.2147/DDDT.S320320
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: Berberine Encapsulated Lecithin-Chitosan Nanoparticles as Innovative Wound Healing Agent in Type II Diabetes.

    Panda, Dibya Sundar / Eid, Hussein M / Elkomy, Mohammed H / Khames, Ahmed / Hassan, Randa M / Abo El-Ela, Fatma I / Yassin, Heba A

    Pharmaceutics

    2021  Band 13, Heft 8

    Abstract: The aim of this research is to formulate a lecithin-chitosan based nanoparticulate system loaded with berberine (BER-LC-CTS-NPs) that could be integrated into a topically applied formulation and assessed for healing wounds in a diabetic animal model. In ... ...

    Abstract The aim of this research is to formulate a lecithin-chitosan based nanoparticulate system loaded with berberine (BER-LC-CTS-NPs) that could be integrated into a topically applied formulation and assessed for healing wounds in a diabetic animal model. In order to formulate BER-LC-CTS-NPs, soybean lecithin, isopropyl myristate, and berberine dispersed in ethanolic solution were added into an aqueous solution of chitosan dropwise with sonication. We assessed the influence of lecithin amount, chitosan amount, and isopropyl myristate concentration on particle diameter, zeta potential, and entrapment and employed a Box-Behnken statistical design. The resulting optimized BER-LC-CTS-NPs had a mean size of 168.4 nm, a surface charge of 33.1 mV, and entrapment of 82.3%. The optimized BER-LC-CTS-NPs showed a sustained in vitro release profile. Furthermore, the potential of the optimized BER-LC-CTS-NPs integrated into a topical gel formulation for wound healing in streptozocin-induced diabetic rats was assessed. Our findings show that combining chitosan and berberine in the nanoparticles produces a synergistic effect when it comes to wound healing. The optimized nanoparticulate system works by reducing inflammation, inducing blood vessels and fibroblast proliferation, and promoting mature collagen fibers deposition. Based on the experimental results, lecithin-chitosan nanoparticles loaded with berberine have evolved as a promising strategy for accelerating wound the healing process in diabetic patients. However, the clinical merits of the developed system need to be investigated in diabetic patients.
    Sprache Englisch
    Erscheinungsdatum 2021-08-04
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2527217-2
    ISSN 1999-4923
    ISSN 1999-4923
    DOI 10.3390/pharmaceutics13081197
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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