Adaptive Batch Size Image Merging Steganography and Quantized Gaussian Image Steganography

2020 ◽  
Vol 15 ◽  
pp. 867-879 ◽  
Author(s):  
Mehdi Sharifzadeh ◽  
Mohammed Aloraini ◽  
Dan Schonfeld
Keyword(s):  
Image Steganography ◽  
Batch Size ◽  
Gaussian Image ◽  
Image Merging

RGB Frequency Based Image Steganography

2020 ◽  
pp. 549-553
Author(s):  
Himanshu Kumar ◽  
Nitesh Kumar
Keyword(s):  
Image Steganography ◽  
Minimum Number

In this paper, we introduced a new RGB technique for image steganography. In this technique we introduced the idea of storing a different number of bits per channel (R, G or B) of a pixel based on the frequency of color values of pixel. The higher color frequency retains the maximum number of bits and lower color frequency stores the minimum number of bits.

Improved LSB method for Image Steganography using H´enon Chaotic Map

2014 ◽  
Vol 2014 (1) ◽  
pp. 34-42 ◽  
Author(s):  
N. S. Raghava ◽  
◽  
Ashish Kumar ◽  
Aishwarya Deep ◽  
Abhilasha Chahal ◽  
...  
Keyword(s):  
Chaotic Map ◽  
Image Steganography

3 (2) Factorial Design Assisted Crushed Puffed Rice-HPMC-Chitosan based Hydrodynamically Balanced System of Metoprolol Succinate

2020 ◽  
Vol 10 (3) ◽  
pp. 237-249
Author(s):  
Shashank Soni ◽  
Veerma Ram ◽  
Anurag Verma
Keyword(s):  
Drug Release ◽  
Factorial Design ◽  
Hydroxypropyl Methylcellulose ◽  
Batch Size ◽  
Metoprolol Succinate ◽  
Zero Order Kinetics ◽  
Two Factors ◽  
Puffed Rice ◽  
Model Drug

Introduction: Hydrodynamically balanced system (HBS) possesses prolonged and continuous delivery of the drug to the gastrointestinal tract which improves the rate and extent of medications that have a narrow absorption window. The objective of this work was to develop a Hydrodynamically Balanced System (HBS) of Metoprolol Succinate (MS) as a model drug for sustained stomach specific delivery. Materials and Methods: Experimental batches were designed according to 3(2) Taguchi factorial design. A total of 9 batches were prepared for batch size 100 capsules each. Formulations were prepared by physically blending MS with polymers followed by encapsulation into hard gelatin capsule shell of size 0. Polymers used were Low Molecular Weight Chitosan (LMWCH), Crushed Puffed Rice (CPR), and Hydroxypropyl Methylcellulose K15 M (HPMC K15M). Two factors used were buoyancy time (Y1) and time taken for 60% drug release (T60%; Y2). Results: The drug excipient interaction studies were performed by the thermal analysis method which depicts that no drug excipient interaction occurs. In vitro buoyancy studies and drug release studies revealed the efficacy of HBS to remain gastro retentive for a prolonged period and concurrently sustained the release of MS in highly acidic medium. All formulations followed zero-order kinetics. Conclusion: Developed HBS of MS with hydrogel-forming polymers could be an ideal delivery system for sustained stomach specific delivery and would be useful for the cardiac patients where the prolonged therapeutic action is required.

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