As worldwide over-dependence on oil and the costly Iraq war has hastened the way for new energy regimes, the U.S. financial bailout will be hastening the use of economic models other than Darwinian capitalism as it has been known where the most able seize maximum resources for themselves. Nascent social movements for opting out of the traditional economic system will become stronger. Science fiction is rife with dystopian models of robotic controlled governments (Daniel Suarez’ Daemon is a recent example) but in many ways machine-like entities absent the agency problem could be a dramatic improvement over fallible people-administered governments. Technology is more often humanifying than dehumanifying.
As usual, the focus is on technological advances to remedy the current global energy, resource consumption and economic challenges. Given both history and the present status of initiatives, technology is likely to deliver. New eras may be ushered in even more quickly when demand is higher and complacency lower. A surveillance and sousveillance society is clearly emerging, simultaneously from top-down government and corporate programs and bottom-up individual broadcast of GPS location and other lifestreaming. The trend to freeing human time for productive and rewarding initiatives is continuing. What will be the first chicken in every pot, the robotic cleaner or self-cleaning nanosurfaces? How soon can all jobs be outsourced to AI? How soon will there be options on the nucleotide chassis?
Sunday, September 28, 2008
Our beautiful future
Posted by LaBlogga at 9:05 AM View Comments
Labels: artificial intelligence, capitalism, daemon, daniel suarez, economics, energy, financial bailout, future economics, nanotechnology, oil, outsourcing, sousveillance, surveillance
Sunday, September 21, 2008
Synthetic biology advances
The realization of synthetic biology, one of the cornerstone fields in this century’s life science revolutions, is a step closer this year with three important advances.
First, synthetic biology movement leader Drew Endy has arrived at Stanford from MIT. Knowing that people and tools are critical to the area’s development, he is assembling a world class curriculum and department to tackle the challenges of synthetic biology, estimating that Stanford is four years behind.
Second, more than 85 worldwide university teams have entered this year’s iGEM (international genetically engineered machines) competition. 900 students are estimated to be at MIT for the November 8-9 presentation of their work and the contest’s culmination. Previous year’s novel synthetic designs have included wintergreen and banana-scented E. coli bacteria, creating virtual-machine like computational platforms in cells and microbial cameras or light programmable biofilms.
Third, record attendance is expected at the fourth annual Synthetic Biology conference will be taking place October 10-12 at the Hong Kong University of Science and Technology.
Biology investigation, modeling, simulation and building
Synthetic biology is starting to have more process and rigor, particularly as articulated by Martyn Amos in Genesis Machines. Several areas have been simultaneously improving and coming together: biological system and process enumeration, 3D software modeling and simulation, and biological machine building. As CAD and EDA allowed semiconductor designers to achieve new levels of productivity and automate complex circuit design and test, so too are software tools aiding biology.
Bio-SPICE (Biological Simulation Program for Intra- and Inter-Cellular Evaluation) is an open source framework and software toolset for the modeling and simulation of spatio-temporal processes in living cells. The innovation process for synthetic biologists is now:
- investigate the biological phenomenon or mechanisms
- mathematically model the existing or novel phenomenon
- use software simulation to test the model
- build it in the lab with standardized off the shelf biological parts of synthesized DNA
Posted by LaBlogga at 1:15 PM View Comments
Labels: bio-SPICE, biological parts, endy, igem, mathematical modeling, simulation, Standard Registry of Biological Parts, synbio, synthetic biology
Sunday, September 14, 2008
Status of public transport
The second annual Bay Area TransitCamp was an interesting venue for public transportation employees, community representatives, software developers and interested citizens to discuss all manner of subjects relating to public transportation, in particular technical, planning, communications and policy aspects. The informal venue allowed high-quality information sharing, education and brainstorming from multiple viewpoints.
Public transport companies are trying to understand how to improve their service, and communications and interactions with riders and the public in general. Political and other community representatives are trying to understand how to improve transit solutions and decrease local traffic congestion. The upcoming $10 billion California ballot initiative for high-speed rail construction is pointing up what appears to be a lack of coordinated long-term strategic planning and integration of the nine Bay Area transit authorities.
Software developers are working on applications, services and standards.
There are two kinds of transit applications: schedule information and real-time updatesThird party developers like iCaltrain are providing more user-friendly platform-portable schedule information. NextBus is moving to the next layer by providing real-time GPS-enabled vehicle location information and service alerts, nationwide, as transit providers make data available. BART is twittering service alerts and other information. MyBart is overlaying public transit data with event information, discounts and sponsor offerings.
The main Internet-enabled service is the formalization and expansion of ride share and carpool systems. There are already a few dozen of these services such as zimride, Avego, RideNow, eRideShare and GoLoco; for dynamic or planned, local or long-distance rides and already the usual a need for a meta ride share site.
TripML and DynamicRidesharing are two standards efforts under development and promulgation.
Still looks like quite a wait for PRT (personal rapid transit)…
Posted by LaBlogga at 11:49 PM View Comments
Labels: congestion, data apps, environment, living green, mobile data, public transit, standards, transit, transportation
Sunday, September 07, 2008
Cost of each new drug: $1.3 billion
The Tufts Center for the Study of Drug Development¹ estimated that it was costing $1.3 billion in 2006 to bring each new drug to market. Why is it so expensive and why does the cost keep growing precipitously? There have been some technology advances, but they are expensive and have helped to raise the number of discoveries but not the number of approved drugs. Little cost-scaling is available at present for the clinical trial and production process bottlenecks of current drug development.
Biggest cost component: clinical trials
The biggest cost in bringing a new drug to market is human clinical trials, and these costs continue to grow. Without standardized electronic health records and other obvious initiatives, it is time-consuming and costly to source and enroll appropriate clinical trial participants. The cocktail problem is also in effect as people have had more varying health issues and remedies over time. The amount of detail to be collected and assessed increases and homogeneous and isolated factor patient comparisons are more difficult.
Increased complexity and amortization of failed drugs
The low-hanging fruit drugs have already been discovered. The diseases currently studied have less readily identifiable and more complex target molecules in the body. The target molecules have more intricate biological interactions and less easily matchable compounds for therapies. Each successful drug includes the cost of failed drugs as only one in five marketed drugs is able to pay for its R&D costs.
No cost decreases for biologic drugs
One of the main kinds of drugs produced starting in 1998 is biological drugs. These are drugs that mimic the effects of substances naturally made by the body. The fixed time, process and other costs required to produce these genetically engineered substances means that economies of scale do not ensue for larger volumes. This is compared to traditional drugs which became cheaper over time in production, helping to offset the cost of new discoveries.
Unclear benefits of newtech
How can the paradox of technology advances yet constant numbers of approved drugs be explained? Technology advances have been proliferating in areas such as mass spectrometry, protein crystallography, chromatography, flow cytometry, microfluidics, genetic scanning and synthesis and atomic force microscopy, all of which are helpful but expensive. The ongoing cost to maintain a state of the art lab has skyrocketed. Newtech has meant that the rate of discovered substances and medicines in development is increasing (2,700 compounds are in development in 2007 vs. 2,000 in 2003)², but the complete process of creating viable therapies and moving them through clinical trials to approval is the bottleneck.
¹ J.A. Dimasi and H.G. Grabowski, “The Cost of Biopharmaceutical R&D: Is Biotech Different?,” Managerial and Decision Economics 28 (2007): 469-479
² Adis R&D Insight Database, 27 February 2008
Posted by LaBlogga at 3:29 PM View Comments
Labels: biological drug, clinical trials, drug development, drug production, pharmaceutical costs
Sunday, August 31, 2008
The long arm of the corporate agenda
One of the most interesting places to look for social commentary is … in corporate annual reports. The medium is ripe for gaffes, unmasked agendas and misdeeds, for example, Big Oil's unabashed proxy statement solicitations to shareholders each year to vote against greenhouse gas emissions goals and environmental impact reports (documented in this post and comments).
General Mills. America’s processed food provider.
The 'fattening of America' trend has treated General Mills well, the stock is up 15% this year to date (vs. the S&P 500's 12% decline) and up 40% since 2005.
You be the judge - is the General Mills 2008 Annual Report a triumph of demographic marketing or would it be over the top to see it as a perpetuation of racial stereotyping?
The Latina is featured center front with a Fajita product (go Hispanic demographic!). Why is she is the only one sitting? The fit-looking Caucasian woman, in pearls, is holding snack bars (because as a size 2, she is only entitled to diet food?). The African American man is holding nothing (what is the messaging here? General Mills does not have products (or jobs, see back cover) for African Americans?).
Flipping to the back cover, another healthy looking Caucasian woman is holding party mix (sorority alumnae?). The older guy with the paunch is leaning on several cases of sugar-coated cereal, and the balding corporate executive is holding reports, not food items. Only the women and the overweight men have food? Where is that lucrative gay demographic? Or maybe the African American male is doing double duty as a metrosexual.
Inside, the story continues. The Chairman and CEO jauntily appear, strangely without food products, though collegially in shirtsleeves.
Posted by LaBlogga at 12:07 PM View Comments
Labels: agenda, coporate america, fattening of America, marketing, processed food, special interest, stereotype
Sunday, August 24, 2008
Economic fallacies II
Fallacy #3: The singularity is a great investment opportunity
A technological revolution like that brought about by the PC or the Internet is a great investment opportunity. Current possibilities for this kind of compound growth in technology-driven financial returns include alternative energy, genomics, personalized medicine, anti-aging therapies, 3d data manipulation tools and narrowly-applied artificial intelligence.
A technological singularity is not necessarily a great investment opportunity. A technological singularity implies change so radical and diffuse that prior models for understanding and exploiting or profiting from the world will no longer work. There is a substantial risk that financial markets as they are known today could disappear. Growth, alpha and superior financial returns may be irrelevant in a post-traditional financial markets era. Planning for the possibility of a technological singularity suggests a much broader definition of what the assets of the future may be and allocating to these areas, a substantial shift away from the traditional asset preservation and financial returns that outpace inflation in the long-run mindset of today.
Fallacy #4: Economic systems become irrelevant in a post-scarcity economy
This is the notion that economies and markets go away in a post-scarcity economy for material goods. At present, an increasing number of goods and services are becoming available for free or offered via modern business models such as the freemium. In the future, substantially all material needs may be easily met at low cost or for free in a molecular-nanotech society, but scarcity as an economic dynamic is likely to persist and economics systems in general are also likely to continue.
Scarcity would be perceived in whatever material resources were not yet plentifully available and in any finite resources such as time, ideas, attention, emotion, reputation, quality, etc. Economic system dynamics could change substantially, for example, property tax would not make sense in a world where nanotech could rapidly build or absorb structures. Unless economics and markets as the most effective means of resource distribution are superceded, they are likely to endure.
Fallacy #5: Social capital markets need not deliver competitive returns
The conventional notion is that it is acceptable for social capital market investments to deliver lower returns than traditional financial instruments. Social capital market investment products include SRI equity funds, corporate governance initiatives, social capital venturing (private equity), fair trade coffee and organic products. On average, consumers are willing to spend 5% more for attribute products (products with affinity attributes such as fair trade, local, organic, etc.) and investors have been willing to sacrifice 5% or more in financial return for socially responsible investments.
However, after some implementation time lag, social capital could have equal or higher returns. Sustainable socially responsible businesses should be more profitable not less. Both direct tangible economic benefits can accrue as well as the indirect benefits of marketing and market-knowledge that the business is more principled and sustainable. Corporate governance and other green or social initiatives should benefit the bottom line, not penalize it. The notion that return and social good are mutually exclusive is a fallacy.
The article with all nine fallacies is available here
Posted by LaBlogga at 8:04 PM View Comments
Labels: affinity capital, corporate governance, fallacies, freemium, future economics, investing, molecular-nano, post-scarcity economy, scarcity, singularity, social capital, SRI, technology economics
Sunday, August 17, 2008
Fallacies when thinking about the economics of future technology
Future technologies seem so impactful and fabulous that it is easy to jump to incorrect conclusions about what things would be like with their advent.
Fallacy #1: Molecular assemblers will have a worldwide overnight rollout
The conventional assumption is that once humans are able to make one molecular assembler, it will be able to self-replicate, and therefore within twenty-four hours everyone worldwide will have one. It is far more likely that a molecular assembler would follow the usual s-curve adoption pattern of any other newtech; early versions are expensive and clunky with minimal functionality, continued improvement iterations make the newtech more relevant and usable.
The first molecular assemblers may be like a next generation 3d printer, printing the T-shirt a friend sent as an email attachment. Only early adopters will have the utility (read: money and interest) to purchase the first molecular assemblers. Also, the first molecular assemblers will not be able to self-replicate as the intricate molecular manufacturing processes will need to be conducted at special facilities.
Finally, the full newtech ecosystem needs to be considered, while carbon and other basic elements could be obtained easily from dirt piles delivered to suburban driveways, industrial utility solutions are need for the 50% of the urbanized world. Cartridge supply for specialty elements (think Gillette) will be required. Matter decompiling will need to be a feature of the molecular assembler or there will need to be some other means of recycling. More here, here and here.
Fallacy #2: Don’t develop newtech if it’s not cheap enough for universal access
This is the view that we should not develop any beneficial newtech unless it can be immediately accessible worldwide at a low price. “Folks, lets not make the Eniac since not everyone can have one.” However noble this view may be, it again ignores the historical precedent of technology development, rollout and penetration. A fundamental property of technology is that it may be expensive at the outset but then price drops, functionality improvements and re-purposing to new markets occur over time. For example, those currently paying $100,000 a year for life extension treatments are hopefully helping to rationalize, standardize and develop a broader market for these services.
Work can still be done on open-source and universal accessibility models, and diligence applied to clearing public goods to non-IP protected regimes (e.g.; the human genome), but with the understanding that traditional technology development models (cost drops over time) will continue to drive progress.
In fact, there can be benefits in not adopting newtech immediately; costs are higher, unintended consequences are unknown, early adopters can work out the kinks (e.g; the first generation iPhone cost $600, the second generation iPhone 3G with expanded functionality emerged a year later at $199) and older technology generations like landline telephony can be skipped. World-is-flat cycle time speed-ups and new business models (e.g.; OneWorldHealth as a non-profit pharmaceutical company directed at developing world disease) illustrate market efficiency in applying traditional technology development in today’s world.
The article with all nine fallacies is available here
Posted by LaBlogga at 8:00 AM View Comments
Labels: economic fallacies, economics of technology, future economics, future of technology, molecular assembler, nanotechnology, properties of technology, technology rollout, universal access
Sunday, August 10, 2008
Human augmentation via bacterial biome
Human augmentation of physical and mental capabilities by bringing electronics on board seems a likely future. The early stages have already been realized, 10% of Americans are cyborgs today in the sense of having synthetic items permanently implanted: hearing aids, teeth, pacemakers, hip and knee replacements, RFID chips etc. Cochlear implants interfacing with hearing cognition for deaf children are routine. Neuroengineering research has been progressing in the implementation of electroencephalography-based computer controllers. Brain cap video game headsets may become the norm.
There are at least three ways for achieving human-electronic interfaces; physical implants, wearables and a third as yet unconsidered possibility, exploiting the human bacterial biome.
The 1,000 trillion bacteria that are part of each human (10x the number of human cells) could be an ideal augmentation substrate.There are trillions of them, they are already on board and pass easily and unobtrusively in and out of the human. They are easy to obtain, test and experiment on in the lab. They are expendable. Functionality could be enabled individually, or distributed over the 500 – 100,000 classes of bacteria.
Augmentation applications: communications and processing
The two most important augmentation applications are communications and processing, both of which could potentially be conducted via the human’s microscopic bacteria. Communication is required between the bacteria, which they are already doing to some extent, and externally, to the Internet using wireless, Bluetooth or some other, possibly to be developed protocol. What a vast improvement on board connectivity would be, never having to depend on the vagaries of PC wireless cards, modems and Bluetooth devices.
The second main application is processing, the initial killer app being a memory aid. Coordinating the bacterial biome into a distributed biocomputer for searching, downloading, accessing and delivering information would be an obvious first goal. Other applications could include continuous lifelogging perhaps (literally) through eye cam bacteria, personalized biosensing and remediation of the external environment as it interfaces with humans, virtual reality and nutrient and waste cycling. Electricity from the body could possibly facilitate these computations.
Easy upgrade and maintenance
The continual turnover, ingress and egress of bacteria in humans means that upgrade cycles and retirement of dead or non-functioning elements could occur seamlessly. Bacterial updates could be printed regularly from a 3d printer or automatically dispensed in smarthome air or water. Mechanically, the updates might be delivered through the air, in the shower, or by a nutrient blanket during sleep.
Nanobot intermediaries
Enhancing the human bacterial biome would really just be extending the life support functionality it already provides and could be a nice intermediary step to the more robust bionanodevices and nanobots envisioned in molecular manufacturing. Existing bacteria could be enhanced, much of the human microflora does not appear to be doing anything anyway, or additional bacteria could be engineered and brought on board.
Posted by LaBlogga at 2:48 PM View Comments
Labels: augmentation, bacterial biome, biocomputing, cyborg, human augmentation, human-machine interface, neuroengineering
Sunday, August 03, 2008
VC life extension opportunity redux
The VC life extension investment opportunity could happen in at least three areas: first and most importantly, translational medicine, second, health social networks and third, distantly, standardized longevity treatments and delivery systems.
Translational medicine
The biggest and most obvious longevity play for VCs is in translational medicine, shepherding and commercializing science findings from basic research to patient therapies. The vast majority, perhaps even 90% or more, of basic research findings never go beyond the lab or journal publication. A particularly high profile example of an early stage longevity company that rocketed from test tube to IPO to big pharma acquisition is Sirtris, bought by GlaxoSmithKline for $720M in June 2008. Some other early stage translational medicine longevity startups are Elixir Pharmaceuticals, Juvenon and Sierra Sciences. In the plethora of remedies claiming science support, it is critical to tightly link the research evidence to the intervention. For example, in this year’s exploding brain fitness market, there is much claim of scientific support but little published clinical trial evidence.
Health social networks
Another VC play is health social networks (for example, PatientsLikeMe, CureTogether, DailyStrength, HealthChapter, Experience Project and peoplejam). Not only can patients connect and generate group-synthesized, curated and moderated knowledge, but health social networks can also facilitate the development of personalized medicine by being a repository for the quantitative data of genomics, ongoing biomarker measurements and electronic healthcare records. Big pharma can approach patient communities for field studies and clinical trials.
Longevity treatment delivery
Standardized longevity treatments and delivery programs via private clinics are not a traditional VC play, but some interesting 10x business models may be possible. In the several years before longevity treatments are more proven and automatically administered via traditional healthcare channels, these services can be provided by private clinics as they are now.
What would improve the longevity treatment market is standardization; standardization of doctor qualifications, certifications, validations, services and treatments, and treatments supported by scientific research clearly evidenced to consumers. Currently, longevity doctors offer heterogeneous suites of services which is challenging for consumers to parse. Positioned appropriately, there is more than adequate demand despite the current lack of insurance reimbursement. Since longevity treatments are currently outside the purview of traditional medicine, third party certification (for example led by the Methuselah Foundation) could help validate doctors and treatment programs, and contribute to industry standards.
Posted by LaBlogga at 1:54 PM View Comments
Labels: commercializing basic research, health social networks, investing, life extension, longevity, translational medicine, VCs, venture capital
Sunday, July 20, 2008
Next big VC market: life extension?
Life extension is a growing market and could be the next significant industry targeted by Venture Capitalists and private investment as alternative energy and clean tech eventually wane. The opportunity is made obvious by continuous soaring costs in the world’s largest industry, healthcare, unfunded Medicare type liabilities in every industrialized country, and the demographic aging of populations and below replacement fertility rates together with massive demand and willingness to spend on longevity remedies.
What is the Life Extension Market?
The life extension market is the commercialization of scientific findings from stem cell, immunology, cancer, regenerative medicine and other areas of research. The research linkage between products and research will hopefully become stronger and more standardized. For example, many longevity remedies available today claim scientific support. This research could and should be linked to the products online (23andme is a nice example of research linkage) so consumers and other interested parties can research the products themselves. Bloggers and other independent intermediary watchdogs could synthesize the scientific research and confirm or deny the product claims.
Longevity Docs Needed
It is not clear that traditional physicians will be those prescribing longevity remedies. Specialist longevity docs are needed and will likely arise and market themselves as such, there are a few examples of this today. Most traditional physicians do not currently have expertise in new areas such as longevity and personalized genomics, or the enhancement and prevention vs. cure mindset.
Supplements, Hormones and Enzymes
The first step in life extension treatments is supplements, ranging from a daily multivitamin to the 200 or more supplements per day taken by futurist Ray Kurzweil. The next step is hormone and enzyme replacement therapies, which must generally be overseen by a physician. A variety of treatments have been undertaken per the shifting legal climate, not everyone wanting to be restored to the hormonal levels of their twenties and other reasons.
Longevity Social Network
It would be great to have a health social network (HSN), like PatientsLikeMe and CureTogether for the longevity community. First, people could share the different interventions they are trying. Second, they could upload their ongoing bio-marker test data into an aggregated electronic health record, similar to what Google Health is contemplating, to track and possibly share the impact of the interventions. Third, companies with research and therapies targeting this market could contact an aggregated group to propose field studies, clinical trials and offerings. For example, the 23andme Parkinson’s community has been contacted for such research.
Posted by LaBlogga at 10:00 AM View Comments
Labels: 23andme, enhancement, health social networks, hormone replacement, life extension, longevity, longevity docs, prevention, supplements, VCs




